FDA.reportPublic FDA data

ZONSEN Roll-On Antiperspirant

Manufacturer
Wuhan Zonsen Medical Products Co., Ltd.
Effective date
2024-08-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:17:50

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#

Warnings

WARNINGS SECTION

For external use only

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 4.5%

PURPOSE

OTC - PURPOSE SECTION

Antiperspirant

USE

OTC - PURPOSE SECTION

Reduces underarm perspiration.

DO NOT USE

OTC - DO NOT USE SECTION

on broken skin.

Stop use

OTC - STOP USE SECTION

if rash or irritation occurs.

Ask Doctor Before Use

OTC - ASK DOCTOR SECTION

if you have kidney disease.

Directions

INDICATIONS & USAGE SECTION

Apply to underarms only

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

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 SECTION

Use daily for best results.

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Roll-On AntiperspirantRoll-On Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72932-012-01ZONSEN Roll-On Antiperspirant44 mL in 1 BOTTLELOTION442

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72932-012ZONSEN ROLL-ON ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LOTION [WUHAN ZONSEN MEDICAL PRODUCTS CO., LTD.]2Current NDC, 1 package rows20240828_2032bd55-a9f8-651e-e063-6394a90ab110.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72932-01272932-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPIACT
DIMETHICONE92RU3N3Y1OIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
STEARIC ACID4ELV7Z65APIACT
PROPYLPARABENZ8IX2SC1OHIACT
GLYCERINPDC6A3C0OXIACT
TRIETHYLAMINEVOU728O6AYIACT
POLYSORBATE 60CAL22UVI4MIACT
SORBITAN MONOSTEARATENVZ4I0H58XIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
METHYLPARABENA2I8C7HI9TIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT

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.2032bd55-a9f8-651e-e063-6394a90ab1102024-08-26WarningsExact identifier
ndc (package): 72932-012-01
ndc (product): 72932-012
ndc11 (package): 72932001201
spl id: 20a12eb9-4d4a-b359-e063-6394a90a2ec7
spl set id: 2032bd55-a9f8-651e-e063-6394a90ab110

Reported adverse events (FAERS/openFDA)#

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