Suave
FDA Label NDC 64942-1459
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 64942-1459). 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
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?
call toll-free 1-800-782-8301
Packaging
Image Description (Suave)
* Please review the disclaimer below.
