FDA.reportPublic FDA data

Alcohol Hand Sanitizer

Manufacturer
Guangdong bangze medicine co., ltd
Effective date
2026-01-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:32:53

Label at a glance#

ProductAlcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

●Place enough product in your palm to thoroughly spread onboth hands and rub into the skin until dry. ●Children under 6 years of age should be supervised when using this porduct.

Storage and handling

●Store below 106'F (41°C) ●May discolor certain fabrics or surfaces ●Validity period after opening: 12 months

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60%

Purpose

OTC - PURPOSE SECTION

Antimicrobia

Use

INDICATIONS & USAGE SECTION

Handsanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use near the eyesIn case of contact, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

When using this product, do not use near the eyesln case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop useand askadoctorifir ritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keepout of reach of children. If swallowed, get medical help orcontacta
Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

●Place enough product in your palm to thoroughly spread
onboth hands and rub into the skin until dry.
●Children under 6 years of age should be supervised when
using this porduct.

Other information

STORAGE AND HANDLING SECTION

●Store below 106'F (41°C)
●May discolor certain fabrics or surfaces
●Validity period after opening: 12 months

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Dandelion Extract, Winter FlowerExtract, Aminomethyl Propanol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039483ethanol 60 % Topical SolutionPSN3
1039483ethanol 0.6 ML/ML Topical SolutionSCD3
1039483ethanol 60 % Topical SolutionSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85279-001-01Alcohol Hand Sanitizer30 mL in 1 BOTTLELIQUID303

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
85279-00185279-001-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
CARBOMER0A5MM307FCIACT
WATER059QF0KO0RIACT
TARAXACUM OFFICINALE (DANDELION) ROOT9DE5YCO0RUIACT
AMINOMETHYL PROPANOLLU49E6626QIACT
TUSSILAGO FARFARA LEAFG2GH7V846ZIACT
ALCOHOL3K9958V90MACTIB

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
Alcohol Hand SanitizerALCOHOL HAND SANITIZERGuangdong bangze medicine co., ltd2e8b5afe-6ff8-3e9b-e063-6394a90ad7032026-01-14WarningsExact identifier
ndc (package): 85279-001-01
ndc (product): 85279-001
ndc11 (package): 85279000101
spl id: 4854f7a2-ac29-882a-e063-6394a90ab8de
spl set id: 2e8b5afe-6ff8-3e9b-e063-6394a90ad703

Reported adverse events (FAERS/openFDA)#

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