DEODORANT ANTIPERSPIRANT SPRAY 80ml

Manufacturer
Shengnan (Guangzhou) Cosmetics Co., LTD
Effective date
2024-12-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:49:27

Label at a glance#

ProductDEODORANTANTIPERSPIRANTSPRAY
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Please keep out of reach of children.

OTC - PURPOSE SECTION

Reduces sweat production and keeps skin dry. While inhibiting sweat, it also prevents odor, ensuring a fresh body scent.

OTC - STOP USE SECTION

Discontinue use if skin shows abnormalreactions.A patch test on a small areaof skin is recommended before full use.

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate

OTC - WHEN USING SECTION

Please keep your skin dry before use to ensure the best results fromthe product.

INACTIVE INGREDIENT SECTION

Butylene Glycol
Propylene Glycol
Alcohol
Water
Fragrance
Algin
Agar
Titanium Dioxide
Pentylene Glycol
Polyoxyethylene Cetyl Stearyl Diether
Stearic Acid
C12-16 Alcohols
Phenoxyethanol
Menthol
Salvia Miltiorrhiza Root Extract
Eugenia Caryophyllus (Clove) Bud Extract
Angelica Polymorpha Sinensis Root Extract
Centella Asiatica Extract
Glycyrrhiza Uralensis (Licorice) Root Extract
Jojoba Esters
CI 26100

DOSAGE & ADMINISTRATION SECTION

Apply 2 times a day

INDICATIONS & USAGE SECTION

Hold the bottle about 15 cm away fromthe underarm and spray evenly ontoclean, dry skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1212

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84019-022-01DEODORANTANTIPERSPIRANTSPRAY80 mL in 1 BOTTLELIQUID801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84019-022DEODORANTANTIPERSPIRANTSPRAY (ALUMINUM CHLOROHYDRATE) LIQUID [SHENGNAN (GUANGZHOU) COSMETICS CO., LTD]11 package rows20241229_2a5199e7-30e2-2c52-e063-6394a90a0c83.zip

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
84019-02284019-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
2a5199e7-30e3-2c52-e063-6394a90a0c832a5199e7-30e2-2c52-e063-6394a90a0c832024-12-28WarningsExact identifier
spl id: 2a5199e7-30e3-2c52-e063-6394a90a0c83
spl set id: 2a5199e7-30e2-2c52-e063-6394a90a0c83

Reported adverse events (FAERS/openFDA)#

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