FDA.reportPublic FDA data

PAU Disposable Hand Sanitizer

Manufacturer
Guangzhou Baoli Cosmetics Co., Ltd.
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:26

Label at a glance#

ProductPAU Disposable Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65%±5% (V/V)

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help decrease bacteria on the skin and recommended for repeated use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Warnings:

WARNINGS SECTION

  • For external use only.
  • Flammable.
  • Keep away from fire or flame.
  • Do not apply around eyes.
  • Do not use in ears and mouth.

When using this product, Avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if irritation or rash appears on the skin.

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands rub together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other Information: 

  • Do not store above 85℉.
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aminomethyul Propanol, Carbomer.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136920268214565GTIN-13: 6920268214565
EAN-13: 6920268214565
GTIN storage (14 digits): 06920268214565		pau disposable hand sanitizer 4 sizes.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75255-004-012021-07-23C16284748780-1c7ccaba7-266a-fd44-e053-dadaa90aa01bf1b6af29-b1bc-4672-86be-567cd8e702fc
75255-004-022021-07-23C16284748780-1c7ccaba7-266a-fd44-e053-dadaa90aa01bf1b6af29-b1bc-4672-86be-567cd8e702fc
75255-004-032021-07-23C16284748780-1c7ccaba7-266a-fd44-e053-dadaa90aa01bf1b6af29-b1bc-4672-86be-567cd8e702fc
75255-004-042021-07-23C16284748780-1c7ccaba7-266a-fd44-e053-dadaa90aa01bf1b6af29-b1bc-4672-86be-567cd8e702fc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75255-004-01PAU Disposable Hand Sanitizer60 mL in 1 BOTTLESOLUTION601
75255-004-02PAU Disposable Hand Sanitizer100 mL in 1 BOTTLESOLUTION1001
75255-004-03PAU Disposable Hand Sanitizer250 mL in 1 BOTTLESOLUTION2501
75255-004-04PAU Disposable Hand Sanitizer480 mL in 1 BOTTLESOLUTION4801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75255-004PAU DISPOSABLE HAND SANITIZER (ALCOHOL) SOLUTION [GUANGZHOU BAOLI COSMETICS CO., LTD.]1Legacy NDC, 4 package rows20200514_f1b6af29-b1bc-4672-86be-567cd8e702fc.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75255-00475255-004-01, 75255-004-02, 75255-004-03, 75255-004-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
water059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER 934Z135WT9208IACT

Source Document#

Source XML · Source PDF

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
26f21511-8fff-4fb0-b6fc-bc463297d0e0f1b6af29-b1bc-4672-86be-567cd8e702fc2020-05-14WarningsExact identifier
spl id: 26f21511-8fff-4fb0-b6fc-bc463297d0e0
spl set id: f1b6af29-b1bc-4672-86be-567cd8e702fc

Reported adverse events (FAERS/openFDA)#

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