Warnings
For external use only
Zonsen Roll-on Antiperspirant Lotion
FDA Label NDC 72932-012
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 Roll-on Antiperspirant (NDC 72932-012). 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 warnings, active ingredient, purpose, use, do not use, stop use, ask doctor before use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Aluminum Chlorohydrate 4.5%
Purpose
Antiperspirant
Use
Reduces underarm perspiration.
Do Not Use
on broken skin.
Stop Use
if rash or irritation occurs.
Ask Doctor Before Use
if you have kidney disease.
Directions
Apply to underarms only
Keep Out Of Reach Of Children
If accidently swallowed, get medical help or contact Poison Control Center right away
Inactive Ingredient
Water, Stearic acid, Mineral Oil, Sorbitan Monostearate, Cetylstearyl Alcohol, Dimethicone, Glyceryl stearate, Butylated Hydroxytoluene, Methylparaben, Propylparaben, Glycerin, Hydroxyethyl cellulose,Disodium EDTA, Tween-60, Triethylamine, Diazolidinyl Urea, Fragrance
Dosage & Administration
Use daily for best results.
Package Label
Roll-on Antiperspirant (Zszhj03 Rollonantiperspirant)
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