Drug Facts

OTC - ACTIVE INGREDIENT SECTION

PHENAZOPYRIDINE HYDROCHLORIDE   97.5 MG

PURPOSE

PHENAZOPYRIDINE HYDROCHLORIDE                     URINARY ANALGESIC

WARNINGS

DO NOT EXCEED RECOMMENDED DOSAGE

ASK DOCTOR

ASK DOCTOR BEFORE USE IF YOU HAVE KIDNEY DISEASEALLERGIES TO FOODS,PRESERVATIVES OR DYESHAD A HYPERSENSITIVE REACTION TO PHENAZOPYRIDINE

WHEN USING

WHEN USING THIS PRODUCT STOMACH UPSET MAY OCCUR,TAKING THIS PRODUCT WITH OR AFTER MEALS MAY REDUCE STOMACH UPSETYOUR URINE WILL BECOME REDDISH ORANGE IN COLOR.THIS IS NOT HARMFUL,BUT CARE SHOULD BE TAKEN TOAVOID STAINING CLOTHING OR OTHER ITEMS.

STOP USE

STOP USE AND ASK A DOCTORIF YOUR SYMPTOMS LAST FOR MORE THAN 2 DAYSYOU SUSPECT YOU ARE HAVING AN ADVERSE REACTION TO THE MEDICATION

PREGNANCY OR BREAST FEEDING

ASK A HEALTH PROFESSIONAL BEFORE US

KEEP OUT OF REACH OF CHILDREN

IN CASE OF OVERDOSE ,GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

INDICATIONS & USAGE

Use; fast relief from urinary pain,burning,urgency and frequency associated with urinary tract infections.

INACTIVE INGREDIENT

Lactose, magnesium silicate, magnesium stearate, microcrystalline cellulose,pharmaceutical glaze, and sodium starch glycolate.

DOSAGE & ADMINISTRATION

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.

HOW SUPPLIED

NDC: 71335-1661-1: 6 Tablets in a BOTTLE

NDC: 71335-1661-2: 12 Tablets in a BOTTLE

NDC: 71335-1661-3: 36 Tablets in a BOTTLE

NDC: 71335-1661-4: 20 Tablets in a BOTTLE

NDC: 71335-1661-5: 10 Tablets in a BOTTLE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Phenazopyridine Hcl 97.5mg Tablet