FDA.reportPublic FDA data

ZONSEN Clear Antiperspirant Deodorant

Manufacturer
Wuhan Zonsen Medical Products Co., Ltd.
Effective date
2025-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:10

Label at a glance#

ProductZONSEN Clear Antiperspirant Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure12 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 7.8%

Do not use

OTC - DO NOT USE SECTION

on broken skin.

Stop use

OTC - STOP USE SECTION

if rash or irritation occurs.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have kidney disease.

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

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

Warnings

WARNINGS SECTION

For external use only.

Directions

INDICATIONS & USAGE SECTION

Apply to underarms only.

Use

OTC - PURPOSE SECTION

Reduces underarm perspiration.

Dosage

DOSAGE & ADMINISTRATION SECTION

Use daily for best results.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZONSEN

PERSONAL CARE

Clear Antiperspirant Deodorant

FRESH SCENT

0.1 FL. OZ.(3ml)

ZSZHJ06 Clear Antiperspirant DeodorantZSZHJ06 Clear Antiperspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72932-017-01ZONSEN Clear Antiperspirant Deodorant3 mL in 1 PACKETLOTION31

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
72932-01772932-017-01

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
METHYLPARABENA2I8C7HI9TIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
GLYCERINPDC6A3C0OXIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
HYDROXYPROPYL METHYLCELLULOSE3NXW29V3WOIACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
TRIETHYLAMINEVOU728O6AYIACT

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
5aefed89-7291-0886-e063-6294a90a1f6c36a62fc4-3786-94f3-e063-6394a90acdbd2026-09-07WarningsExact identifier
spl set id: 36a62fc4-3786-94f3-e063-6394a90acdbd

Reported adverse events (FAERS/openFDA)#

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