Otc - Active Ingredient
PHENAZOPYRIDINE HYDROCHLORIDE 97.5 MG
The following Structured Product Label (SPL) was submitted to the FDA by Walgreens Co. for the product Walgreens Urinary Pain Relief Maximum Strength (NDC 0363-0113). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, warnings, otc - ask doctor, otc - when using, otc - stop use, otc - pregnancy or breast feeding, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
PHENAZOPYRIDINE HYDROCHLORIDE 97.5 MG
PHENAZOPYRIDINE HYDROCHLORIDE URINARY ANALGESIC
DO NOT EXCEED RECOMMENDED DOSAGE
ASK DOCTOR BEFORE USE
IF YOU HAVE KIDNEY DISEASE
ALLERGIES TO FOODS,PRESERVATIVES OR DYES
HAD A HYPERSENSITIVE REACTION TO PHENAZOPYRIDINE
WHEN USING THIS PRODUCT
STOMACH UPSET MAY OCCUR,TAKING THIS PRODUCT WITH OR AFTER MEALS MAY REDUCE STOMACH UPSET
YOUR URINE WILL BECOME REDDISH ORANGE IN COLOR.THIS IS NOT HARMFUL,BUT CARE SHOULD BE TAKEN TO
AVOID STAINING CLOTHING OR OTHER ITEMS.
STOP USE AND ASK A DOCTOR
IF YOUR SYMPTOMS LAST FOR MORE THAN 2 DAYS
YOU SUSPECT YOU ARE HAVING AN ADVERSE REACTION TO THE MEDICATION
ASK A HEALTH PROFESSIONAL BEFORE USE
IN CASE OF OVERDOSE ,GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Use; fast relief from urinary pain,burning,urgency and frequency associated with urinary tract infections.
Lactose, magnesium silicate, magnesium stearate, microcrystalline cellulose,
pharmaceutical glaze, and sodium starch glycolate.
Adults and Children 12 years of age and over; take 2 tablets 3 times daily with a full glass of water,with or after meals as needed.
Children under 12 years of age; consult a doctor.
Do not use for more than 2 days ( 12 tablets ) without consulting a Doctor.
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