FDA.reportPublic FDA data

ZONSEN Roll-On Antiperspirant

Manufacturer
Wuhan Zonsen Medical Products Co., Ltd.
Effective date
2024-08-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:17:41

Label at a glance#

ProductZONSEN Roll-On Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure12 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Antiperspirant

Use

OTC - PURPOSE SECTION

Reduces underarm perspiration.

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 7.8%

OTC - DO NOT USE SECTION

on broken skin.

DISCONTINUE USE IF

OTC - WHEN USING SECTION

■irritation and redness develop

■ If condition persists for more than 72 hours consult a doctor.

Warnings

WARNINGS SECTION

For external use only

Directions

INDICATIONS & USAGE SECTION

Apply to underarms only.

ASK A DOCTOR BEFORE USE

OTC - ASK DOCTOR SECTION

if you have kidney disease.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water, PEG-40 Hydrogenated Castor Oil, Diazolidinyl Urea, Hydroxyproply Methyl Cellulose, Glycerin, Methylparaben, Disodium EDTA,Triethylamine, Fragrance

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Use daily for best results.

BOTTLE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZONSEN TM

PERSONAL CARE

Clear Roll-On
Antiperspirant

FRESH SCENT

1.5 FL. OZ. (44ml)

Clear Roll-On AntiperspirantClear Roll-On Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72932-014-01ZONSEN Roll-On Antiperspirant44 mL in 1 BOTTLELOTION441

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72932-014ZONSEN ROLL-ON ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LOTION [WUHAN ZONSEN MEDICAL PRODUCTS CO., LTD.]1Current NDC, 1 package rows20240824_203375a3-50db-7c1e-e063-6394a90a4039.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72932-01472932-014-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
METHYLPARABENA2I8C7HI9TIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
HYPROMELLOSES3NXW29V3WOIACT
EDETATE DISODIUM7FLD91C86KIACT
GLYCERINPDC6A3C0OXIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
TRIETHYLAMINEVOU728O6AYIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZONSEN Roll-On AntiperspirantALUMINUM CHLOROHYDRATEWuhan Zonsen Medical Products Co., Ltd.203375a3-50db-7c1e-e063-6394a90a40392024-08-21WarningsExact identifier
ndc (package): 72932-014-01
ndc (product): 72932-014
ndc11 (package): 72932001401
spl id: 203375a3-50dc-7c1e-e063-6394a90a4039
spl set id: 203375a3-50db-7c1e-e063-6394a90a4039

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.