Antiperspirant Deodorant Fresh Women Lotion
FDA Label NDC 53675-163

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 Fresh Women (NDC 53675-163). 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 and 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

→ drug Facts

→ Active Ingredient

→ Purpose

→ Uses:

→ Do Not Use

→ Stop Use And Ask A Doctor

→ Directions:

→ Inactive Ingredients:

→ Package Labeling:

Drug Facts

Active Ingredient

Aluminum Chlorohydrate 16%

Purpose

antiperspirant

Uses:

Reduces underarm perspiration

Do Not Use

on broken skin.

Stop Use And Ask A Doctor

if rash or irritation occurs. Ask a doctor before use if you have kidney disease

Directions:

Apply to underarms only.

Inactive Ingredients:

Water (Aqua/Eau), Glyceryl Stearate, Caprylic/Capric Triglyceride, Ceterateh-20, Ceteareth-21, Cetyl Alcohol, Aloe Barbadensis Leaf Juice (Aloe Vera Gel from Aruba), Fragrance (Parfum), Phenoxyethanol, Caprylyl Glycol, Chlorphenesin.