Dove
FDA Label NDC 64942-1618

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 64942-1618). 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 dove dermacare scalp coconut hydration anti-dandruff conditioner - pyrithione zinc liquid, drug facts, 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

Drug Facts

Active ingredient
Pyrithione Zinc (0.5%)

Purpose

Anti-dandruff

Use

• Helps prevent and control recurrence of itching and flaking associated with dandruff.

Warning

• For external use only
• When using this product: Avoid contact with eyes. If contact occurs, rinse eyes thoroughtly 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. Massage into scalp and hair. Rinse.

Inactive Ingredients

Water(Aqua), Cetearyl Alcohol, Cyclopentasiloxne, Stearamidopropyl Dimethylamine, Dimethiconol, Behentrimonium Chloride, Cocos Nucifera(Coconut)Oil, Citrus Aurantifolia (Lime) Juice, Tocopheryl Acetate, Panthenol, Fragrance(Parfum), Dipropylene Glycol, Lactic Acid, DMDM Hydantoin, Zinc Sulfate, Sodium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, PEG-150 Distearate.

Questions?

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