Antiperspirant moisturizer

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-10-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:24:09

Label at a glance#

ProductAntiperspirant moisturizer
Active ingredientALOE VERA LEAF
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice

Inactive ingredient

INACTIVE INGREDIENT SECTION

Niacinamide,Simmondsia Chinensis (Jojoba) Seed Oil, Avena Sativa (Oat) Kernel Extract, Ethylene/Propylene Styrene Copolymer, Jojoba Wax PEG-120 Esters

Purpose section

OTC - PURPOSE SECTION

1. Provides a targeted solution tocontrol sweat accumulation, providingdrier, more comfortable skin.

2. Uses carefully selected activeingredients to minimize sweatproduction on the face (forehead,nose, upper lip and other facial areasprone to sweating)

Warning

WARNINGS SECTION

1. Please use according to theinstructions.

2. lf it accidentally gets into your eyes,please rinse with water immediately.

3. lf there are any abnormalities onyour skin, please stop using it.

4. Please keep out of reach of children.Prevent children from accidentallyswallowing, and pregnant womenshould use with caution.

stop use

OTC - STOP USE SECTION

This product may cause allergic reactions in asmall number of people.
lf youexperience 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

1. Cleanse your face and dry it.

2. Take a small amount ofthis productand apply evenly on the foreheadand other parts prone to sweating

3. Wait for it to dry naturally for 2minutes, and then use it with otherskin care products as needed

Dosage

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-038-012025-07-29C16284748780-13b156c62-2e28-fb37-e063-e6dba90a4e07241baa99-978e-4720-e063-6394a90ac818

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-038-01Antiperspirant moisturizer50 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-038ANTIPERSPIRANT MOISTURIZER CREAM [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20241012_241baa99-978e-4720-e063-6394a90ac818.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84732-03884732-038-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
241baa99-978f-4720-e063-6394a90ac818241baa99-978e-4720-e063-6394a90ac8182024-10-10WarningsExact identifier
spl id: 241baa99-978f-4720-e063-6394a90ac818
spl set id: 241baa99-978e-4720-e063-6394a90ac818

Reported adverse events (FAERS/openFDA)#

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