Otc - Active Ingredient
Active Ingredients Purpose
Aluminum Chlorohydrate 12.3% Antiperspirant
Antiperspirant Deodorant Roll-on
FDA Label NDC 68828-198
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jafra Cosmetics International for the product Antiperspirant Deodorant Roll-on (NDC 68828-198). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses
Reduces underarm wetness
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
Stop use if rash or irritation occurs
Warnings
Warnings
For external use only
Do not use on broken skin
Ask a doctor before use if you have kidney disease
Dosage & Administration
apply to underarms only
Inactive Ingredient
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
Package Label.Principal Display Panel
Jafra Daily
antiperspirant
deodorant
roll-on
60 ml 2 Fl Oz (US)
Antiperspirant Carton (Dailyantideoroll On)
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