Active Ingredient
Aluminum Chlorohydrate 12.3%
Jafra Daily Skin Brightening Antiperspirant Deodorant Roll-on Liquid
FDA Label NDC 68828-759
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 Skin Brightening Antiperspirant Deodorant Roll-on (NDC 68828-759). 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 - keep out of reach of children, directions, inactive ingredients, 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 Ingredients
Water/Aqua, PEG-40 Stearate, Stearic Acid, PEG-25 Propylene Glycol Stearate, Cetyl Alcohol, Magnesium Aluminum Silicate, Sorbitan Sesquioleate, Fragrance/Parfum, Phenoxyethanol, Ehtylhexylhexylglycerin, Mica, Titanium Dioxide/CI 77891, Azadirachta Indica Extract, Curcuma Longa Extract, Hemisdesmus Indicus Extract, Sphaeranthus Indicus Extract, Phyllanthus Emblica Extract, Alpha-Isomethyl Ionone, Benzyl Salicylate, Citronellol, Geraniol, Hexyl Cinnamal, Limonene, Linalool
Product Label
Image Description (Image 01)
Image Description (Image 02)
* Please review the disclaimer below.
