Active Ingredient
Aluminum chlorohydrate 15%
Antiperspirant Deodorant
FDA Label NDC 50636-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Frabel S.a De C.v. for the product Antiperspirant Deodorant (NDC 50636-003). 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 active ingredient, purpose, uses, warnings, otc - pregnancy or breast feeding, otc - keep out of reach of children, directions, drug facts (continued) inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Uses
Reduces underarm perspiration
Warnings
For external use onlyDo not use on broken skin.Stop use if rash or irritation occurs.Ask a doctor before use if you have kidney disease
Otc - Pregnancy Or Breast Feeding
If pregnant or breast-feeding, ask a health professional before use.
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
Drug Facts (Continued) Inactive Ingredients
Water, corn starch, cetearyl alcohol, fragrance, dimethicone, linalool, alpha-isomethyl ionone, geraniol, ceteareth-33, butylphenyl methylpropional, citronellol
Package Label
Package Label
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