Suave
FDA Label NDC 64942-1457

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 Suave (NDC 64942-1457). 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.

Drug Facts

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20 %)

Purpose

anti-perspirant

Uses

• reduces underarm wetness • 24 hour protection • extra effective

Warnings

•  For external use only
•  Do not use on broken skin.
•  Ask a doctor before using 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

 •   before bed, apply two to three clicks of product to each underarm

Inactive Ingredients

Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Fragrance (Parfum), Silica, Dimethicone Crosspolymer, BHT

Questions?

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Packaging

Suave (Suave)

Suave (Suave)

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