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Distributed by Owens & Minor
9120 Lockwood Blvd.
Mechanicsville, VA 23116
Roll-on Antiperspirant Deodorant - Scented Solution
FDA Label NDC 39892-0807
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by O&m Halyard, Inc. for the product Roll-on Antiperspirant Deodorant - Scented (NDC 39892-0807). 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, otc - keep out of reach of children, otc - do not use, 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, 10%-Anhydrous Basis
Purpose
Antiperspirant
Use
Reduces underarm wetness.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. For external use only.
Otc - Do Not Use
Do not use on broken skin. Stop use if rash or irritation occurs. 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 only. Use daily for best results.
Inactive Ingredients
Purified Water, Hydroxyethyl Cellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA
Principal Display Panel
MEDICHOICE®
ROLL-ON
ANTIPERSPIRANT
DEODORANT
CLEAN FRESH SCENT
FIGHTS WETNESS
1.5 fl. oz. (45 mL.)
Principal Display Panel (45 mL Bottle Label)
* Please review the disclaimer below.
