Suave Powder Roll-On Antiperspirant Deodorant - Aluminum Chlorohydrate Liquid
Suave Powder Roll-On AntiPerspirant Deodorant
Suave
FDA Label NDC 64942-1852
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 64942-1852). 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 suave powder roll-on antiperspirant deodorant - aluminum chlorohydrate liquid, drug facts, 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 Chlorohydrate (17.6%)
Purpose
antiperspirant
Uses
• reduces underarm wetness
• 24 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
Water (Aqua), PPG-11 Stearyl Ether, Steareth-2, Steareth-20, Fragrance (Parfum), Glycerin.
Questions?
Call toll-free 1-800-782-8301
Package
Suave Powderrolllonapdeo (Suavepowderrollonapdeo)
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