Otc - Active Ingredient
Active ingredients Purpose
Aluminum Chlorohydrate 12.3% Antiperspirant
Skin Brightening Antiperspirant Deodorant Roll-on
FDA Label NDC 68828-199
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 Skin Brightening Antiperspirant Deodorant Roll-on (NDC 68828-199). 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 before use if you have kidney disease
Dosage & Administration
Directions
Apply to underarms only
Inactive Ingredient
Water/Aqua, PEG-40 Stearate, PEG-25 Propylene Glycol Stearate, Cetyl Alcohol, Magnesium Aluminum Silicate, Sorbitan Sesquioleate, Fragrance/parfum, Phenoxyethanol, Ehtylhexylhexyl Glycerin, Mica, Titanium Dioxide/CI 77891, Azadirachta Indica Extract, Curcuma Longa, Hemisdesmus Indicus, Sphaeranthus Indicus Extract, Phyllanthus Emblica Extract
Package Label.Principal Display Panel
Jafra
Daily
Skin Brightening
antiperspirant deodorant roll-on
60 ml 2 FL OZ
Carton (Dayn 041ucdailybrighteningroll Onusa)
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