FDA Label for Equaline Dandruff Dry Scalp 2 In 1
View Indications, Usage & Precautions
Equaline Dandruff Dry Scalp 2 In 1 Product Label
The following document was submitted to the FDA by the labeler of this product Supervalu Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
PYRITHIONE ZINC 1%
Purpose
ANTI-DANDRUFF
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.
Uses
HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF
Directions
FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRE.
Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Zinc Carbonate, Glycol Distearate, Dimethicone, Fragrance (Parfum), Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Benzyl Alcohol, Sodium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Xylenesulfonate
Package Front And Back Labels
14OZ Front and Back Labels: eql14.jpg
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