Dove
FDA Label NDC 64942-1486
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conopco, Inc. D/b/a/ Unilever for the product Dove (NDC 64942-1486). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, use, warning, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Pyrithione Zinc (0.5%)
Purpose
Anti-dandruff
Use
Helps prevent and control recurrence of itching, flaking and irritation 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.
Otc - Keep Out Of Reach Of Children
Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
For best results use at least twice per week or as directed by a doctor. After shampooing, massage into scalp and hair. Rinse.
Inactive Ingredients
Water(Aqua), Cetearyl Alcohol, Cyclopentasiloxne, Stearamidopropyl Dimethylamine, Dimethiconol, Behentrimonium Chloride, Cocos Nucifera(Coconut)Oil, Butyrospermum Parkii(Shea)Butter, Tocopheryl Acetate, Helianthus Annuus(Sunflower)Seed Oil, Fragrance(Parfum), Dipropylene Glycol, Lactic Acid, DMDM Hydantoin, Zinc Sulfate, Sodium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, PEG-150 Distearate
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