Skopko Urinary Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Skopko Urinary Pain Relief

Skopko
Reese Pharmaceutical Co

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Phenazopyridine Hydrochloride 95 mg

Purpose

Urinary Analgesic

Skopko Urinary Pain Relief Uses

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

Warning

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

■ 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  

If pregnant or breast feeding

ask a health professional before use.

Keep out of the reach of children

in case of an overdose,get medical help or contact a Poison Control Center right away.

Directions


■ Adults and children 12 and over: take 2 tablets 3 times daily with a full glass of water, with or after meals as needed
Children under 12: consult a doctor
Do not use for more than 2 days (12 tablets) without consulting a doctor

Inactive Ingredients

magnesium stearate,microcrystalline cellulose.May also contain carnauba wax,

croscarmellose sodium,hypromellose,lactose,magnesium silicate,maize starch,pharmaceutical

glaze,polyethylene glycol,povidone,pregelatinized starch,sodium starch glycolate.

Skopko Urinary Pain Relief

Skopko Urinary Pain Relief

PHENAZOPYRIDINE HYDROCHLORIDE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37012-098
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHENAZOPYRIDINE HYDROCHLORIDE PHENAZOPYRIDINE 95 mg

Inactive Ingredients

Ingredient Name Strength
MAGNESIUM STEARATE
cellulose, microcrystalline
carnauba wax
CROSCARMELLOSE SODIUM
HYPROMELLOSES
LACTOSE
magnesium silicate

Product Characteristics

Color Size Imprint Code Shape
red 7 mm CPC64 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37012-098-50 32 in 1 CELLO PACK
2 NDC:37012-098-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-07-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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