Active Ingredient
Aluminum Chlorohydrate 4.5%
Zonsen Roll-on Antiperspirant Lotion
FDA Label NDC 72932-013
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 72932-013). 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 active ingredient, purpose, use, warnings, do not use, stop use, ask doctor before use, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
Reduces underarm perspiration.
Warnings
For external use only
Do Not Use
on broken skin.
Stop Use
if rash or irritation occurs.
Ask 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
Directions
Apply to underarms only.
Inactive Ingredient
Water, Stearic acid, Mineral Oil, Sorbitan Monostearate, Cetylstearyl Alcohol, Dimethicone, Glyceryl stearate, Butylated Hydroxytoluene, Methyl paraben, Propylparaben, Glycerin, Hydroxyethyl cellulose, Disodium EDTA, Tween-60, Triethylamine, Diazolidinyl Urea
Dosage & Administration
Use daily for best results.
Package Label
Roll-on Antiperspirant (Zszhj04 Rollonantiperspirant)
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