Dove
FDA Label NDC 64942-1479

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 64942-1479). 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, uses, warnings, 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

Aluminum Zirconium Tetrachlorohydrex GLY (15.2%)

Purpose

anti-perspirant

Uses

  • Reduces Underarm Wetness
  • 48 Hour Protection

Warnings

For external use only.

Do not use on broken skin.

Ask a doctor before use if you have kidney disease.

Stop use if rash or irritation occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply to underarms only

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, PEG-8, Fragrance (Parfum), Dimethicone, Silica, Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Talc, Sea salt, PEG-4, steareth-100, BHT.

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