Purpose
Antiperspirant
Zonsen Roll-on Antiperspirant Lotion
FDA Label NDC 72932-014
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 72932-014). 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, use, active ingredient, otc - do not use, discontinue use if, warnings, directions, ask a doctor before use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
Reduces underarm perspiration.
Active Ingredient
Aluminum Chlorohydrate 7.8%
Otc - Do Not Use
on broken skin.
Discontinue Use If
â– irritation and redness develop
â– If condition persists for more than 72 hours consult a doctor.
Warnings
For external use only
Directions
Apply to underarms only.
Ask A Doctor Before Use
if you have kidney disease.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact Poison Control Center right away
Inactive Ingredient
Water, PEG-40 Hydrogenated Castor Oil, Diazolidinyl Urea, Hydroxyproply Methyl Cellulose, Glycerin, Methylparaben, Disodium EDTA,Triethylamine, Fragrance
Dosage & Administration
Use daily for best results.
Bottle Label
ZONSEN TM
PERSONAL CARE
Clear Roll-On
Antiperspirant
FRESH SCENT
1.5 FL. OZ. (44ml)
Clear Roll-on Antiperspirant (Rd7990 Rollonantiperspirant)
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