Equaline Dandruff description, usages, side effects, indications, overdosage, supplying and lots more!

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Equaline Dandruff

Supervalu Inc

Drug Facts Box - Back Label


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

PYRITHIONE ZINC 1%

PURPOSE

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF

CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER IMMEDIATELY.


Equaline Dandruff Uses

Directions

Inactive Ingredients

Water (Aqua), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Zinc Carbonate, Glycol Distearate, Dimethicone, Fragrance (Parfum), Cetyl Alcohol, Guar Hydroxypropyltrimonium Chloride, Magnesium Sulfate, Sodium Benzoate, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Benzyl Alcohol, Sodium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Xylene Sulfonate, Blue 1 (CI 42090), Red 4 (CI 14700), Yellow 10 (CI 47005).

Package Front and Back Labels

eql14.jpgEqualine Dandruff

Equaline Dandruff

PYRITHIONE ZINC SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41163-413
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC 1 mL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41163-413-14 420 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2010-09-16


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