Dove Clinical Protection Visibly Smooth Wild Rose
FDA Label NDC 64942-1074

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 Clinical Protection Visibly Smooth Wild Rose (NDC 64942-1074). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20%)

Otc - Purpose

Purposeanti-perspirant

Indications & Usage

Uses·  reduces underarm wetness·  24 hour protection·  extra effective

Warnings

WarningsFor external use only

Otc - Do Not Use

Do not use on broken skin

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease

Otc - Stop Use

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.

Dosage & Administration

Directions·  apply to underarms only·  before bed, apply three clicks of product to each underarm

Inactive Ingredient

Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Fragrance (Parfum), Silica, Stearyl Alcohol, Helianthus Annuus  (Sunflower) Seed Oil, Dimethicone Crosspolymer, Nylon-12, Sorbitan Laurate, BHT, Palmatine, Red 40 Lake (CI 16035)

Otc - Questions

Questions?  Call toll-free 1-800-761-DOVE

Package Label.Principal Display Panel

1.7 oz PDP
1.7 oz carton

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