Antiperspirant gel

Manufacturer: Dongguan Haiyi Technology Co.,Ltd.
Effective date: 2024-10-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:26:42

Label at a glance#

ProductAntiperspirant gel

Active ingredientALUMINUM CHLOROHYDRATE

Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate

Inactive ingredient

INACTIVE INGREDIENT SECTION

aqua ,alcohol, Glycerin, Mentha Piperita Oil

Purpose section

OTC - PURPOSE SECTION

Refreshing and antiperspirant, long-lasting odor-free,gentle and safe, non-irritating, the bestchoice for your skin, suitable for sensitive skin

Warning

WARNINGS SECTION

1. For external use, do not put into themouth or eyes. lf it gets into the eyesaccidentally, please rinse with clean waterimmediately. lf you feel discomfort, pleasestop using it. Do not use it on irritated ordamaged parts.

2. Keep out of reach of children.

3. Seal after use and place in a cool andventilated place, avoid sunlight.

stop use

OTC - STOP USE SECTION

This product may cause allergic reactions in as mall number of people.
lf you experience any discomfort,please stop using it immediately.

not use

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breast feeding people.

OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

INDICATIONS & USAGE SECTION

Take an appropriate amount of this product and spray it directly on the required area

Dosage

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
84732-052-01	2025-07-29	C162847	48780-1	3b156c62-29ca-fb37-e063-e6dba90a4e07	24a7340b-4f4e-25b4-e063-6394a90a2238

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84732-052-01	Antiperspirant gel	50 mL in 1 BOTTLE, PUMP	GEL	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
84732-052	ANTIPERSPIRANT GEL GEL [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]	1	1 package rows	20241019_24a7340b-4f4e-25b4-e063-6394a90a2238.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Antiperspirant gel
ALUMINUM CHLOROHYDRATE
WATER
ALCOHOL
GLYCERIN
PEPPERMINT OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84732-052	84732-052-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
GLYCERIN	PDC6A3C0OX	IACT
PEPPERMINT OIL	AV092KU4JH	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
24a7340b-4f4f-25b4-e063-6394a90a2238			24a7340b-4f4e-25b4-e063-6394a90a2238	2024-10-17	Warnings	Exact identifier spl id: 24a7340b-4f4f-25b4-e063-6394a90a2238 spl set id: 24a7340b-4f4e-25b4-e063-6394a90a2238

Reported adverse events (FAERS/openFDA)#

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