Other
Drug Facts
Distributed by: NWI, Inc.
Nashville, TN 37228
Freshscent Anti-perspirant Deodorant Solution
FDA Label NDC 51824-022
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by New World Imports, Inc. for the product Freshscent Anti-perspirant Deodorant (NDC 51824-022). 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.
Otc - When Using
If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.
Directions
Apply to underarms only.
Inactive Ingredients
Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Tetrasodium EDTA
Principal Display Panel
freshscent™
UNSCENTED
Roll-On
Antiperspirant Deodorant
2 FL. OZ. Principal Display Panel (59 ml Bottle Label)
(59 ml) 
* Please review the disclaimer below.
