Otc - Active Ingredient
Active Ingredient
Aluminum Zirconium Tetrachlorohydrex GLY (20%)
Suave
FDA Label NDC 64942-1037
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 64942-1037). 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, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
anti-perspirant
Warnings
Warnings
For 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.
Indications & Usage
Uses
▪ reduces underarm wetness
▪ 24 hour protection
▪ extra effective
Dosage & Administration
Directions
▪ apply to underarms only
▪ before bed, apply two clicks of product to each underarm
Inactive Ingredient
Inactive ingredients Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Silica, Fragrance (Parfum), Dimethicone Crosspolymer, BHT.
Otc - Questions
Questions? Call toll-free 1-800-782-8301
1.7 Oz Carton
Suaveclinicalpowdercarton (Suaveclinicalpowdercarton)
* Please review the disclaimer below.
