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Drug Facts
Roll On Anti-perspirant (alcohol Free) Solution
FDA Label NDC 63517-803
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health for the product Roll On Anti-perspirant (alcohol Free) (NDC 63517-803). 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 other, active ingredient, purpose, use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Aluminum Chlorohydrate 10% - Anhydrous Basis
Purpose
Antiperspirant
Use
Reduces underarm wetness.
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease.
Otc - Stop Use
Stop use if rash or irritation occurs.
Otc - Keep Out Of Reach Of Children
Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.
Directions
Apply to underarms only.
Inactive Ingredients
Fragrance, Glycerin, Hydroxyethylcellulose, Polysorbate 20, Purified Water, Tetrasodium EDTA
Principal Display Panel
NDC 63517-803-45
deodorant +
antiperspirant
roll-on • scented
CardinalHealth
1.5 fl oz (45ml)
Principal Display Panel (45ml Bottle Label)
* Please review the disclaimer below.
