FDA.reportPublic FDA data

DERMFREE Whole Body Deodorant

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:40:40

Label at a glance#

ProductDERMFREE Whole Body Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure12 sections

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 9%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

.Reduces underamm sweat
.24 hour effective protection

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken skin

When Using

OTC - WHEN USING SECTION

Apply to underarms only

Stop Use

OTC - STOP USE SECTION

rash or irritation occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use ifyou have kidney disease

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Ifswallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cetyl alcohol,deionized water, glycerin, GLYCERYL MONOOLEATE,GLYCERYL MONOSTEARATE,GR-270773 PHOSPHOLIPID EMULSION, Silicone Oil, zinc phenolsulfonateetc

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974603690552GTIN-13: 6974603690552
EAN-13: 6974603690552
GTIN storage (14 digits): 06974603690552		Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-01584010-015-01

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
GLYCERYL MONOOLEATEC4YAD5F5G6IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
CETYL ALCOHOL936JST6JCNIACT
WATER059QF0KO0RIACT
ZINC PHENOLSULFONATE4O71YT5YB5IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
GR-270773 PHOSPHOLIPID EMULSIOND4B2F53PBHIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERINPDC6A3C0OXIACT

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
4a4700e9-7b3a-27a7-e063-6394a90a4ab0174b55b8-d7ac-90f2-e063-6294a90ab5152026-02-07WarningsExact identifier
spl set id: 174b55b8-d7ac-90f2-e063-6294a90ab515

Reported adverse events (FAERS/openFDA)#

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