Otc - Active Ingredient
Active Ingredient(s)
Aluminum Chlorohydrate 12.3%
Jafra Daily Antiperspirant Deodorant Roll-on Liquid
FDA Label NDC 68828-702
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Distribuidora Comercial Jafra, S.a. De C.v. for the product Jafra Daily Antiperspirant Deodorant Roll-on (NDC 68828-702). 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, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredient, product label, 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 wetness
Warnings
For external use only
Do not use on broken skin
Stop use if rash or irritation occurs
Ask a doctor before use if you have kidney disease
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 Ingredient
Inactive Ingredients
Water/Aqua, PEG-40 Stearate, PEG-25 Propylene Glycol Stearate, Stearic Acid, Sorbitan Sesquioleate, Cetyl Alcohol, Magnesium Aluminum Silicate, Fragrance/Parfum, DMDM Hydantoin, Iodopropynyl Butylcarbamate
Product Label
Image Description (Image 002)
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