Sunmark Urinary Pain Relief Maximum Strength description, usages, side effects, indications, overdosage, supplying and lots more!

Sunmark Urinary Pain Relief Maximum Strength

McKesson
Reese Pharmaceutical Co

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts



FULL PRESCRIBING INFORMATION

Active ingredient

PHENAZOPYRIDINE HYDROCHLORIDE   97.5 MG

Purpose

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 US

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

Uses

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.

Sunmark Urinary Pain Relief Maximum Strength

PHENAZOPYRIDINE HYDROCHLORIDE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-941
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHENAZOPYRIDINE HYDROCHLORIDE PHENAZOPYRIDINE 97.5 mg

Inactive Ingredients

Ingredient Name Strength
LACTOSE
magnesium silicate
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
red 7 mm 975 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-941-02 12 in 1 BLISTER PACK
2 NDC:49348-941-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-09-10


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.