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Nuvicare-Urinary Tract Defense

Dosage form
TABLET
Labeler
NUVICARE LLC
Label updated
2026-08-10
Retrieved
2026-09-07
Active ingredients
METHENAMINE · SODIUM SALICYLATE
View original label and images on DailyMed ↗
Active ingredients (in each tablet)

Methenamine 162 mg

Sodium Salicylate 162.5 mg (NSAID Non steroidal anti-inflammatory drug)

Purpose

Methenamine ................................................................................................................................ Antibacterial
Sodium Salicylate (NSAID Non steroidal anti-inflammatory drug).................................. Analgesic (pain reliever)

Uses

Temporarily relieves:

■Pain & burning ■ frequency and urgency of urination

Warnings

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. If changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

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

■ take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen or others)

■ have 3 or more alcoholic drinks every day while using this product

■ have stomach ulcers or bleeding problems
■ take a blood thinning (anticoagulant) or steroid drug

■are age 60 or older

■take more or for a longer time than directed

Label information

Do not use: if you are on a sodium restricted diet

■ if you are allergic to salicylates (including aspirin) unless directed by a doctor

■ if you have stomach problems (such as heartburn, upset stomach, or stomach pain) that persist or recur, or if you have ulcers or bleeding problems unless directed by a doctor

Label information

Label information

Ask a doctor before use if you have:

■ frequent, burning urination for the first time

■ the stomach bleeding warning applying to you

■ history of stomach problems, such as heartburnm

■ high blood pressure

■ heart disease
■ liver cirrhosis

■ bleeding problems

■ diuretic use

■ ulcers

■ kidney disease

■ reached age 60 or older

Label information

Ask a doctor or pharmacist before use if you are:

■ taking any other drug containing an NSAID (prescription or nonprescription)

■ taking a blood thinning (anticoagulant), steroid, diabetes, gout or arthritis drug

Label information

When using this product: do not take more than the recommended dosage

Label information

Stop use and ask a doctor if:

■ product has been used for 3 days

■ you experience any of the following signs of stomach bleeding:

■ feel faint, vomit blood

■ have blood or black stools

■ have stomach pain that does not get better
■ ringing in the ears or a loss of hearing occurs

Label information

If pregnant or breast-feeding, ask a health professional before use.

Label information

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222)
right away.

Directions

Adults and children 12 years and over: take 2 tablets with a full glass of water 3 times a day. Drink plenty of fluids.

Children under 12 years: ask a doctor.

Other information

■ each tablet contains 23.76 mg of sodium

■ store at 59°F-86°F (15°C-30°C) in a dry place

■ protect from light

Inactive ingredients

benzoic acid, croscarmellose sodium, FD&C red number 40 lake, FD&C yellow number 6 lake, ferrosoferric oxide, hydroxypropyl cellulose, hypromellose, magnesium stearate, methacrylic acid and ethyl acrylate copolymer, powdered cellulose, silicon dioxide, stearic acid, titanium dioxide, triethyl citrate

Questions or comments?

Call +1 (718) 337-8733 or email: [email protected]

Label information

†This product is neither manufactured nor distributed by i-Health, Inc., the distributor of AZO Urinary Tract Defense®

Distributed by: Nuvicare LLC., Brooklyn, NY 11211, U.S.A.
www.nuvicare.com

NDC 84324-041-01

[Image in the official label — see DailyMed source]

DailyMed Set ID: 2ea2717e-437e-4417-a09d-ea7be9d9707d · Version 1
NDC: 84324-041