Purpose
Antiperspirant
Zonsen Clear Antiperspirant Deodorant Lotion
FDA Label NDC 72932-017
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wuhan Zonsen Medical Products Co., Ltd. for the product Zonsen Clear Antiperspirant Deodorant (NDC 72932-017). 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 purpose, active ingredient, do not use, stop use, ask a doctor before use, keep out of reach of children, inactive ingredient, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Aluminum Chlorohydrate 7.8%
Do Not Use
on broken skin.
Stop Use
if rash or irritation occurs.
Ask A Doctor Before Use
if you have kidney disease.
Keep Out Of Reach Of Children
If accidently swallowed, get medical help or contact Poison Control Center right away.
Inactive Ingredient
Diazolidinyl Urea, Disodium EDTA, Fragrance, Glycerin, Hydroxyproply MethylCellulose, Methylparaben, PEG-40 Hydrogenated Castor Oil, Triethylamine, Water
Warnings
For external use only.
Directions
Apply to underarms only.
Use
Reduces underarm perspiration.
Dosage
Use daily for best results.
Label
ZONSEN
PERSONAL CARE
Clear Antiperspirant Deodorant
FRESH SCENT
0.1 FL. OZ.(3ml)
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