Dr Sweat Clinical Strength Antiperspirant - Aluminum Chloride Liquid
Dr Sweat Clinical Strength Antiperspirant
Dr Sweat
FDA Label NDC 64942-1633
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a/ Unilever for the product Dr Sweat (NDC 64942-1633). 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 dr sweat clinical strength antiperspirant - aluminum chloride liquid, drug facts, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Drug Facts
Active ingredient
Aluminum Chloride (15.0%)
Purpose
Antiperspirant
Uses
• reduces underarm perspiration
Warnings
• For externaluse only.
• Do not use on broken skin
.
• Ask a doctor before use if you have
kidney disease.
• 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 right away.
Directions
• Apply to underarms only
• Apply to clean dry underarms before going to bed.
Inactive Ingredients
Water (Aqua), Tetrahydroxypropyl Ethylenediamine, VP/Polycarbamyl Polyglycol Ester, Phenoxyethanol, Polyacrylate Crosspolymer-6
Questions?
Call toll-free 866-269-6082
Other Safety Information
• Highest sweat profession available without a prescription
• Clinically tested and proven formula
• Simply and easy to apply
• No fragrance or alcohol
• Reduces sweat and odor
Packaging
Drsweat (Drsweatpaint)
* Please review the disclaimer below.
