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Generic Name: phenazopyridine (Oral route)

fen-ay-zoe-PIR-i-deen

Commonly used brand name(s)

In the U.S.

  • Azo-Gesic
  • Azo-Septic
  • Azo-Standard
  • Baridium
  • Phenazo 95
  • Prodium
  • Pyridiate
  • Pyridium
  • RE-Azo
  • Urinary Pain Relief
  • Uristat
  • UTI Relief

Available Dosage Forms:

  • Tablet
  • Kit

Therapeutic Class: Analgesic

Uses For Uristat

Phenazopyridine is used to relieve the pain, burning, and discomfort caused by infection or irritation of the urinary tract. It is not an antibiotic and will not cure the infection itself.

In the U.S., phenazopyridine is available only with your doctor's prescription.

Before Using Uristat

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

Pediatric

Although there is no specific information comparing use of phenazopyridine in children with use in other age groups, it is not expected to cause different side effects or problems in children than it does in adults.

Geriatric

Many medicines have not been studied specifically in older people. Therefore, it may not be known whether they work exactly the same way they do in younger adults. Although there is no specific information comparing use of phenazopyridine in the elderl

tramadol hydrochloride
Dosage Form: tablet, extended release
ULTRAM® ER
(tramadol HCl) Extended-Release Tablets

Rx only

Prescribing Information

Ultram ER Description

ULTRAM® ER (tramadol hydrochloride) is a centrally acting synthetic analgesic in an extended-release formulation. The chemical name is (±) cis-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl) cyclohexanol hydrochloride. Its structural formula is:

Figure 1

The molecular weight of tramadol HCl is 299.8. It is a white, bitter, crystalline and odorless powder that is readily soluble in water and ethanol and has a pKa of 9.41. The n-octanol/water log partition coefficient (logP) is 1.35 at pH 7. Ultram ER tablets contain 100, 200 or 300 mg of tramadol HCl in an extended-release formulation. The tablets are white to off-white in color and contain the inactive ingredients ethylcellulose, dibutyl sebacate, polyvinyl pyrrolidone, sodium stearyl fumarate, colloidal silicon dioxide, and polyvinyl alcohol.

Ultram ER - Clinical Pharmacology

Mechanism of Action

Ultram ER is a centrally acting synthetic opioid analgesic. Although its mode of action is not completely understood, from animal tests, at least two complementary mechanisms appear applicable: binding of parent and M1 metabolite to µ-opioid receptors and weak inhibition of reuptake of norepinephrine and serotonin.

Opioid activity is due to both low affinity binding of the parent compound and higher affinity binding of the O-demethylated metabolite M1 to µ-opioid receptors. In animal models, M1 is up to 6 times more potent than tramadol in producing analgesia and 200 times more potent in µ-opioid binding. Tramadol-

Pronunciation: un-deh-sil-EN-ik AS-id/klor-oh-ZYE-le-nole
Generic Name: Undecylenic Acid/Chloroxylenol
Brand Name: Gordochom

Undecylenic Acid/Chloroxylenol is used for:

Treating athlete's foot and ringworm. It may also be used for other conditions as determined by your doctor.

Undecylenic Acid/Chloroxylenol is an antifungal. It works by preventing fungal growth.

Do NOT use Undecylenic Acid/Chloroxylenol if:

  • you are allergic to any ingredient in Undecylenic Acid/Chloroxylenol

Contact your doctor or health care provider right away if any of these apply to you.

Before using Undecylenic Acid/Chloroxylenol:

Some medical conditions may interact with Undecylenic Acid/Chloroxylenol. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

  • if you are pregnant, planning to become pregnant, or are breast-feeding
  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
  • if you have allergies to medicines, foods, or other substances
  • if you have diabetes or blood vessel problems in your arms or legs

Some MEDICINES MAY INTERACT with Undecylenic Acid/Chloroxylenol. Because little, if any, of Undecylenic Acid/Chloroxylenol is absorbed into the blood, the risk of interacting with another medicine is low.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Undecylenic Acid/Chloroxylenol may interact with other medicines that you take. Check with your health care provider before you start, stop, or chan

Pronunciation: ue-REE-a/SOE-dee-um HYE-al-ure ON-ate
Generic Name: Urea
Brand Name: Umecta PD

Umecta PD Topical Suspension is used for:

Promoting the healing of certain skin conditions (eg, hyperkeratotic conditions). It may also be used for certain other skin conditions (eg, corns; calluses; rough, dry skin) as determined by your doctor.

Umecta PD Topical Suspension contains a debriding agent and an emollient. The debriding agent works by helping the breakdown of dead skin and pus, which helps to loosen and shed hard and scaly skin. The emollient moisturizes and softens the skin.

Do NOT use Umecta PD Topical Suspension if:

  • you are allergic to any ingredient in Umecta PD Topical Suspension

Contact your doctor or health care provider right away if any of these apply to you.

Before using Umecta PD Topical Suspension:

Some medical conditions may interact with Umecta PD Topical Suspension. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

  • if you are pregnant, planning to become pregnant, or are breast-feeding
  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
  • if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Umecta PD Topical Suspension. Because little, if any, of Umecta PD Topical Suspension is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if Umecta PD Topical Suspension may interact with other medicines that you take. Check with y

Generic Name: loperamide hydrochloride
Dosage Form: tablet
Target Corp. Anti-Diarrheal Drug Facts

Active ingredient (in each caplet)

Loperamide HCl 2 mg

Purpose

Anti-diarrheal

Uses

controls symptoms of diarrhea, including Travelers’ Diarrhea

Warnings

Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide HCl

Do not use

if you have bloody or black stool

Ask a doctor before use if you have

  • fever
  • mucus in the stool
  • a history of liver disease

Ask a doctor or pharmacist before use if you are

taking antibiotics

When using this product

  • tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery.
Pronunciation: ue-REE-a/HYE-al-ure-ON-ik AS-id
Generic Name: Urea Nail Film and Hyaluronic Acid
Brand Name: Umecta

Umecta Nail Film is used for:

Treating damaged or ingrown nails. It may also be used for certain other conditions as determined by your doctor.

Umecta Nail Film is a kit that contains a debriding agent and an emollient. It works by helping to soften and loosen hard, scaly skin or nails.

Do NOT use Umecta Nail Film if:

  • you are allergic to any ingredient in Umecta Nail Film

Contact your doctor or health care provider right away if any of these apply to you.

Before using Umecta Nail Film:

Some medical conditions may interact with Umecta Nail Film. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

  • if you are pregnant, planning to become pregnant, or are breast-feeding
  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
  • if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Umecta Nail Film. However, no specific interactions with Umecta Nail Film are known at this time.

Ask your health care provider if Umecta Nail Film may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Umecta Nail Film:

Use Umecta Nail Film as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Generic Name: potassium citrate (Oral route)

poe-TAS-ee-um SIT-rate

Commonly used brand name(s)

In the U.S.

  • Urocit-K 10
  • Urocit-K 15
  • Urocit-K 5

Available Dosage Forms:

  • Patch, Extended Release
  • Tablet, Extended Release
  • Tablet
  • Solution

Therapeutic Class: Urinary Alkalinizer

Uses For Urocit-K 5

Potassium citrate is used to treat a kidney stone condition called renal tubular acidosis. It is also used to prevent kidney stones that may occur with gout.

Potassium citrate is a urinary alkalinizer. It works by making the urine more alkaline (less acid).

This medicine is available only with your doctor's prescription.

Before Using Urocit-K 5

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

Pediatric

Appropriate studies have not been performed on the relationship of age to the effects of potassium citrate in the pediatric population. Safety and efficacy have not been established.

Geriatric

No information is available on the relationship of age to the effects of potassium citrate in geriatric patients.

Pregnancy

Pregnancy Category Explanation
All Trimesters C Animal studies have shown an adverse effect and there are no a

Dosage Form: liquid
Target Corp. Children's All Day Allergy Relief Drug Facts

Active ingredient (in each 5 mL teaspoonful)

Cetirizine HCl 5 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itchy, watery eyes
  • itching of the nose or throat

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product

  • drowsiness may occur avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
Pronunciation: poe-TASS-ee-um
Generic Name: Potassium Citrate
Brand Name: Urocit-K

Urocit-K is used for:

Preventing certain types of kidney stones. It also may be used for other conditions as determined by your doctor.

Urocit-K is a urinary alkalinizing agent. It works by neutralizing some of the acid in the urine, which helps reduce the formation of crystals.

Do NOT use Urocit-K if:

  • you are allergic to any ingredient in Urocit-K
  • you have high potassium levels in the blood or aluminum toxicity
  • you have stomach ulcers, kidney disease, heart disease, a blockage in the intestines, or a urinary tract infection
  • you are currently taking aldosterone-blockers (eg, eplerenone), aluminum salts (eg, aluminum hydroxide), potassium-sparing diuretics (eg, triamterene), or anticholinergics (eg, atropine)

Contact your doctor or health care provider right away if any of these apply to you.

Before using Urocit-K:

Some medical conditions may interact with Urocit-K. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

  • if you are pregnant, planning to become pregnant, or are breast-feeding
  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
  • if you have allergies to medicines, foods, or other substances
  • if you have heart problems, kidney problems, difficulty swallowing, a stomach blockage, or diabetes
  • if you have dia
Ursodiol
Dosage Form: tablet, film coated
FULL PRESCRIBING INFORMATION

Indications and Usage

Urso 250® and Urso Forte® (Ursodiol) tablets are indicated for the treatment of patients with primary biliary cirrhosis (PBC).

Dosage and Administration

General Dosing Information

The recommended adult dosage for Urso 250® and Urso Forte® in the treatment of PBC is 13-15 mg/kg/day administered in two to four divided doses with food. Dosing regimen should be adjusted according to each patient’s need at the discretion of the physician.

Scoring the Urso Forte Tablet

The Urso Forte scored tablet can be broken in halves to provide recommended dosage.

To break Urso Forte scored tablet easily, place the tablet on a flat surface with the scored section on top. Hold the tablet with your thumbs placed close to the scored part of the tablet (groove). Then apply gentle pressure and snap the tablet segments apart (segments breaking incorrectly should not be used). The segments should be washed down unchewed, with water, keeping the segments in the mouth can reveal a bitter taste. Due to the bitter taste, segments should be stored separately from whole tablets. [see How Supplied/Storage and Handling (16.2)].

Dosage Forms and Strengths

  • Urso 250: 250 mg tablet
  • Urso Forte: 500 mg scored tablet

Contraindications

Known hypersensitivity or intolerance to Ursodiol or any of the components of the formulation.

Warnings and Preca

Generic Name: hyoscyamine, methenamine, methylene blue, and phenyl salicylate (HYE oh SYE a meen, meth EN a meen, METH il een BLUE, FEEN il sa LIS il ate)
Brand Names: Darpaz, Hyophen, Phosenamine, Phosphasal, Prosed/DS, Urelle, Uribel, Uro Blue, Ustell, Uta, UTICAP, Utira, Utira-C

What is Utira (hyoscyamine, methenamine, methylene blue, and phenyl salicylate)?

Hyoscyamine produces many effects in the body, including relief from muscle spasms.

Methenamine and methylene blue work as mild antiseptics that fight bacteria in the urine and bladder.

Phenyl salicylate is a mild pain reliever.

The combination of hyoscyamine, methenamine, methylene blue, and phenyl salicylate is used to treat bladder irritation (pain, burning, inflammation) caused by urinary tract infection. This medication is also used to prevent bladder discomfort during a medical procedure.

Hyoscyamine, methenamine, methylene blue, and phenyl salicylate may also be used for purposes not listed in this medication guide.

What is the most important information I should know about Utira (hyoscyamine, methenamine, methylene blue, and phenyl salicylate)?

You should not use hyoscyamine, methenamine, methylene blue, and phenyl salicylate if you are allergic to it.

Before taking this medication, tell your doctor if you have any type of heart problem (congestive heart failure, coronary heart disease, a heart valve or heart rhythm disorder), glaucoma, an enlarged prostate, bladder obstruction, myasthenia gravis, a stomach ulcer or obstruction, or if you are allergic to belladonna (Donnatal and others).

Drink plenty of liquids while you are taking this medication. If you have an eye exam and your pupils are dilated with eye drops, tell the eye doctor ahead of time that you are using hyoscyamine, methenamine, methylene blue, and phenyl salicylate.

Many drugs c

Generic Name: potassium citrate (Oral route)

poe-TAS-ee-um SIT-rate

Commonly used brand name(s)

In the U.S.

  • Urocit-K 10
  • Urocit-K 15
  • Urocit-K 5

Available Dosage Forms:

  • Patch, Extended Release
  • Tablet, Extended Release
  • Tablet
  • Solution

Therapeutic Class: Urinary Alkalinizer

Uses For Urocit-K 15

Potassium citrate is used to treat a kidney stone condition called renal tubular acidosis. It is also used to prevent kidney stones that may occur with gout.

Potassium citrate is a urinary alkalinizer. It works by making the urine more alkaline (less acid).

This medicine is available only with your doctor's prescription.

Before Using Urocit-K 15

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

Allergies

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

Pediatric

Appropriate studies have not been performed on the relationship of age to the effects of potassium citrate in the pediatric population. Safety and efficacy have not been established.

Geriatric

No information is available on the relationship of age to the effects of potassium citrate in geriatric patients.

Pregnancy

Pregnancy Category Explanation
All Trimesters C Animal studies have shown an adverse effect and there are no
Pronunciation: ue-REE-a/a-MOE-nee-um LAK-tate
Generic Name: Urea in Ammonium Lactate
Brand Name: Examples include Ultralytic 2 and Uramaxin

Urea in Ammonium Lactate Foam is used for:

Treating dry, rough, scaly skin caused by certain conditions (eg, dermatitis, psoriasis, eczema, cracked skin, calluses). It may also be used for certain other skin or nail conditions as determined by your doctor.

Urea in Ammonium Lactate Foam is a keratolytic. It works by helping the breakdown of dead skin, which helps to loosen and shed hard and scaly skin. It also softens and moisturizes the skin.

Do NOT use Urea in Ammonium Lactate Foam if:

  • you are allergic to any ingredient in Urea in Ammonium Lactate Foam

Contact your doctor or health care provider right away if any of these apply to you.

Before using Urea in Ammonium Lactate Foam:

Some medical conditions may interact with Urea in Ammonium Lactate Foam. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

  • if you are pregnant, planning to become pregnant, or are breast-feeding
  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
  • if you have allergies to medicines, foods, or other substances
  • if the affected area is broken or severely irritated

Some MEDICINES MAY INTERACT with Urea in Ammonium Lactate Foam. Because little, if any, of Urea in Ammonium Lactate Foam is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if Urea in Amm

sevoflurane
Dosage Form: volatile liquid for inhalation
Ultane®
(sevoflurane)
volatile liquid for inhalation
NOVAPLUS™

Ultane Description

Ultane (sevoflurane), volatile liquid for inhalation, a nonflammable and nonexplosive liquid administered by vaporization, is a halogenated general inhalation anesthetic drug. Sevoflurane is fluoromethyl 2,2,2,-trifluoro-1-(trifluoromethyl) ethyl ether and its structural formula is:

Sevoflurane, Physical Constants are:

Molecular weight 200.05
Boiling point at 760 mm Hg 58.6°C
Specific gravity at 20°C 1.520 - 1.525
Vapor pressure in mm Hg 157 mm Hg at 20°C
197 mm Hg at 25°C
317 mm Hg at 36°C

Distribution Partition Coefficients at 37°C:

Blood/Gas 0.63 - 0.69
Water/Gas 0.36
Olive Oil/Gas 47 – 54
Brain/Gas 1.15

Mean Component/Gas Partition Coefficients at 25°C for Polymers Used Commonly in Medical Applications:

Conductive rubber 14.0
Butyl rubber
bethanechol chloride
Dosage Form: tablet
Urecholine® TABLETS
(Bethanechol Chloride, USP)

Urecholine Description

Bethanechol chloride, a cholinergic agent, is a synthetic ester which is structurally and pharmacologically related to acetylcholine.

It is designated chemically as 2-[(aminocarbonyl)oxy]-N, N, N-trimethyl-1-propanaminium chloride. Its molecular formula is C7H17CIN202 and its structural formula is:

It is a white, hygroscopic crystalline powder having a slight amine-like odor, freely soluble in water, and has a molecular weight of 196.68.

Each tablet for oral administration contains 5 mg, 10 mg, 25 mg or 50 mg bethanechol chloride, USP. Tablets also contain the following inactive ingredients: anhydrous lactose, colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, and (25 mg and 50 mg) D&C Yellow #10 and FD&C Yellow #6.

Urecholine - Clinical Pharmacology

Bethanechol chloride acts principally by producing the effects of stimulation of the para- sympathetic nervous system. It increases the tone of the detrusor urinae muscle, usually producing a contraction sufficiently strong to initiate micturition and empty the bladder. It stimulates gastric motility, increases gastric tone and often restores impaired rhythmic peristalsis.

Stimulation of the parasympathetic nervous system releases acetylcholine at the nerve endings. When spontaneous stimulation is reduced and therapeutic intervention is required, acetylcholine can be given, but it is rapidly hydrolyzed by cholinesterase and its effects are transient. Bethan- echol chloride

Generic Name: zinc oxide topical (ZINK OX ide)
Brand Names: ARC, Balmex, Boudreaux Butt Paste, Caldesene, Calmol-4 Suppository, Critic-Aid Skin Paste, Delazinc, Dermagran BC, Desitin, Desitin Maximum Strength Original, Desitin Rapid Relief Creamy, Diaper Rash Ointment, Diaper Relief, Dr. Smith's Diaper, Flanders Buttocks Ointment, Geri-Protect, Medi-Paste, PeriGuard, Pinxav, Rash Relief, RVPaque, Seniortopix Healix, Soothe & Cool Skin Paste, Sportz Block Dark, Sportz Block Light, Sportz Block Medium, Triple Paste, Tronolane Suppositories, Unna-Flex Elastic Unna Boot 3 inch, Unna-Flex Elastic Unna Boot 4 inch, Znlin

What is Unna-Flex Elastic Unna Boot 4 inch (zinc oxide topical)?

Zinc oxide is a mineral.

Zinc oxide topical (for the skin) is used to treat diaper rash, minor burns, severely chapped skin, or other minor skin irritations.

Zinc oxide rectal suppositories are used to treat itching, burning, irritation, and other rectal discomfort caused by hemorrhoids or painful bowel movements.

Zinc oxide topical may also be used for purposes not listed in this medication guide.

What is the most important information I should know about Unna-Flex Elastic Unna Boot 4 inch (zinc oxide topical)?

You should not use this medication if you are allergic to zinc, dimethicone, lanolin, cod liver oil, petroleum jelly, parabens, mineral oil, or wax.

Zinc oxide topical will not treat a bacterial or fungal infection. Call your doctor if you have any signs of infection such as redness and warmth or oozing skin lesions.

Keep the diaper area clean and dry to prevent worsening of skin rash. Change wet diapers as soon as possible. Allow the skin to dry thoroughly before putting on a fresh diaper.

Stop using this medication and call your doctor if your condition does not improve within 7 days of treatment. Avoid getting this medica

Class: Thrombolytic Agents
CAS Number: 9039-53-6
Brands: Kinlytic

Introduction

Thrombolytic agent; plasminogen activator isolated from human neonatal kidney cell cultures.111 122 125 136 137 153 155

Uses for Urokinase

PE

Lysis of acute massive PE (obstruction or substantial filling defects of ?2 lobar pulmonary arteries or multiple segments of lungs).111 117 120 132 133 134 136 140 155

Lysis of PE accompanied by unstable hemodynamics (i.e., failure to maintain BP without supportive measures).111 117 120 132 133 134 136 140 155

Generally reserve IV thrombolytic therapy for those with acute massive PE accompanied by unstable hemodynamics (e.g., shock) who do not have major contraindications because of bleeding risk117 120 121 122 132 133 140

Generic Name: ampicillin and sulbactam (am pi SIL in and sul BAK tam)
Brand Names: Unasyn

What is Unasyn (ampicillin and sulbactam)?

Ampicillin and sulbactam are antibiotics in the penicillin group of drugs. They fight bacteria in your body.

The combination of ampicillin and sulbactam is used to treat many different types of infections caused by bacteria.

Ampicillin and sulbactam may also be used for other purposes not listed in this medication guide.

What is the most important information I should know about Unasyn (ampicillin and sulbactam)?

Do not use this medication if you are allergic to ampicillin and sulbactam or to any other penicillin antibiotic, such as amoxicillin (Amoxil), carbenicillin (Geocillin), dicloxacillin (Dycill, Dynapen), oxacillin (Bactocill), penicillin (Beepen-VK, Ledercillin VK, Pen-V, Pen-Vee K, Pfizerpen, V-Cillin K, Veetids), and others.

Before using ampicillin and sulbactam, tell your doctor if you are allergic to cephalosporins such as Ceclor, Ceftin, Duricef, Keflex, and others, or if you have asthma, kidney disease, a bleeding or blood clotting disorder, mononucleosis (also called "mono"), or a history of any type of allergy.

Ampicillin and sulbactam can make birth control pills less effective, which may result in pregnancy. Before using ampicillin and sulbactam, tell your doctor if you use birth control pills. Use this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Ampicillin and sulbactam will not treat a viral infection such as the common cold or flu. Do not give this medication to another person, even if they have the same symptoms you do.

Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or has blood in it, call your doctor. D


Dosage Form: cream
Ultravate®
(halobetasol propionate cream) Cream, 0.05%
For Dermatological Use Only. Not for Ophthalmic Use.
Rx only

Ultravate Cream Description

Ultravate® (halobetasol propionate cream) Cream, 0.05% contains halobetasol propionate, a synthetic corticosteroid for topical dermatological use. The corticosteroids constitute a class of primarily synthetic steroids used topically as an anti-inflammatory and antipruritic agent.

Chemically halobetasol propionate is 21-chloro-6?, 9-difluoro-11?, 17-dihydroxy-16?-methylpregna-1, 4-diene-3-20-dione, 17-propionate, C25H31ClF2O5. It has the following structural formula:

Halobetasol propionate has the molecular weight of 485. It is a white crystalline powder insoluble in water.

Each gram of Ultravate Cream contains 0.5 mg/g of halobetasol propionate in a cream base of cetyl alcohol, glycerin, isopropyl isostearate, isopropyl palmitate, steareth-21, diazolidinyl urea, methylchloroisothiazolinone, (and) methylisothiazolinone and water.

Ultravate Cream - Clinical Pharmacology

Like other topical corticosteroids, halobetasol propionate has anti-inflammatory, antipruritic and vasoconstrictive actions. The mechanism of the anti-inflammatory activity of the topical corticosteroids, in general, is unclear. However, corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, co

Dosage Form: tablet
Target Corp. Naproxen Sodium Tablets, 220 mg Drug Facts

Active ingredient (in each tablet)

Naproxen sodium 220 mg

(naproxen 200 mg) (NSAID)*

*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/fever reducer

Uses

  • temporarily relieves minor aches and pains due to:
  • minor pain of arthritis
  • muscular aches
  • backache
  • menstrual cramps
  • headache
  • toothache
  • the common cold
  • temporarily reduces fever

Warnings

Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

  • hives
  • facial swelling
  • asthma (wheezing)
  • shock
  • skin reddening
  • rash
  • blisters

If an allergic reaction occurs, stop use and seek medical help right away.

Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you

  • are age 60 or older
  • have had stomach ulcers or bleeding problems
  • take a blood thinning (anticoagulant) or steroid drug
  • take other drugs containing prescription or nonprescription NS