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Drug Facts
MFG BY:
HYDROX LABORATORIES
825-B Tollgate Rd. ∙ Elgin, IL 60123
Anti-perspirant Deodorant Roll-on Liquid
FDA Label NDC 10565-074
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hydrox Laboratories for the product Anti-perspirant Deodorant Roll-on (NDC 10565-074). 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, warnings, otc - keep out of reach of children, otc - do not use, otc - stop use, 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.
Warnings
FOR EXTERNAL USE ONLY.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Otc - Do Not Use
Do not use on broken skin.
Otc - Stop Use
Stop use if rash or irritation occurs.
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.
Directions
Apply to underarms. Use daily for best results.
Inactive Ingredients
Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Tetrasodium EDTA
Principal Display Panel - 45 Ml Bottle Label
Personal Care
FreshMoment
Anti-Perspirant
Deodorant Roll-On
Alcohol-Free
Helps Reduce Wetness
FRAGRANCE FREE
Dye Free Formula
MADE IN USA
1.5 FL. OZ. (45mL)
Principal Display Panel (45 mL Bottle Label)
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