FDA Label for Control Anti-dandruff
View Indications, Usage & Precautions
Control Anti-dandruff Product Label
The following document was submitted to the FDA by the labeler of this product Ag Hair Ltd.. 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:
ZINC PYRIDINETHIONE (PYRITHIONE) 2%
Purpose:
Anti-Dandruff
Uses:
HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF.
Warning:
FOR EXTERNAL USE ONLY.
When Using This Product:
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.
Stop Use And Ask A Doctor If:
CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED.
Keep This And All Drugs Out Of Reach Of Children
IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Directions:
- USE TWICE A WEEK, OR AS DIRECTED BY A PHYSICIAN FOR CHRONIC CONDITIONS.
- MASSAGE INTO SCALP FOR 3-5 MINUTES. RINSE THOROUGHLY.
Inactive Ingredients
WATER/AQUA/EAU, AMMONIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE , ALOE BARBADENSIS EXTRACT, CUCUMIS SATIVUS (CUCUMBER) FRUIT EXTRACT, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, SODIUM HYDROXIDE, PANTHENOL, SILK AMINO ACIDS, HYDROLYZED KERATIN, SODIUM PCA, TOCOPHERYL ACETATE, SODIUM HYDROXYMETHYLGLYCINATE, LAURYL PYRROLIDONE, ETHYLHEXYL METHOXYCINNAMATE, CITRIC ACID, PARFUM/FRAGRANCE, MENTHOL, TETRASODIUM EDTA, PROPYLENE GLYCOL, DIAZOLIDINYL UREA, IODOPROPYNYL BUTYLCARBAMATE.
Questions (Or Comments)?
1-866-924-4247
Product Labeling
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