Antiperspirant Deodorant Extra Dry Men Lotion
FDA Label NDC 53675-161
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aruba Aloe Balm Nv for the product Antiperspirant Deodorant Extra Dry Men (NDC 53675-161). 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 drug facts, active ingredient, purpose, uses:, do not use, stop use an ask a doctor, directions:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Aluminum Chlorohydrate 25%
Purpose
antiperspirant
Uses:
Reduces underarm perspiration
Do Not Use
on broken skin.
Stop Use An Ask A Doctor
if rash or irritation occurs. Ask a doctor before use if you have kindney disease.
Directions:
Apply to underarms only.
Inactive Ingredients:
Water (Aqua/Eau), Glyceryl Stearate, Caprylic/Capric Triglyceride, Ceteareth-20, Cetereth-21, Cetyl Alcohol, Aloe Barbadensis Leaf Juice (Aloe Vera Gel from Aruba), Fragrance (Parfum), Phenoxyethanol, Caprylyl Glycol, Chlorphenesin, Propylene Glycol, Methylcellulose.
Package Labeling:
Label (Label)
* Please review the disclaimer below.
