FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Guangzhou BEIEAGLE Technology Co. LTD
Effective date
2020-10-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:17

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly untill dry-children under 6 yeas of age should be supervised when using hand sanitizer

Storage and handling

Store below 43C May discotor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

FLAMMABLE.keep away from fire or flame.
For external use only

When using this product: do not use in or near the eyes.

In case of contact, rinse eyesthoughly with water.

Stop using this product If irritation or rash appears and

lasts

Keep out of reach of children If swallowed, get medical

help or contact a poison control center right away

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

When using this product: do not use in or near the eyes. In case of contact, rinse eyesthoughly with water.

Stop using this product If irritation or rash appears and lasts

Keep out of reach of children If swallowed, get medical help or contact a poison control center right away

OTC - STOP USE SECTION

Stop using this product If irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children If swallowed, get medical help or contact a poison control center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in your palm to cover hands and rub hands together briskly untill dry-children under 6 yeas of age should be supervised when using hand sanitizer

Other information

STORAGE AND HANDLING SECTION

  • Store below 43C
    May discotor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

CARBOMER, ESSENTIAL OIL, GLYCOL, GLYCEROL, WATER, AMP AMINOMETHYL PROPANOL, PERFUME.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80720-001-01 250ml80720-001-01 250ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80720-001-012022-01-28C16284748780-1d6a99b39-e3c9-a426-e053-dadaa90af4c280720-001 HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80720-001-01HAND SANITIZER250 mL in 1 BOTTLEGEL2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80720-001HAND SANITIZER GEL [GUANGZHOU BEIEAGLE TECHNOLOGY CO. LTD]1Legacy NDC, 1 package rows20201009_b125c63a-14a6-0201-e053-2995a90ad0cb.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80720-00180720-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ETHYLENE GLYCOLFC72KVT52FIACT
LAVENDER OILZBP1YXW0H8IACT
GLYCERINPDC6A3C0OXIACT
FAGRAEA BERTEROANA FLOWER90D40Y3CDGIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
AMINOMETHYLPROPANOLLU49E6626QIACT

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
b125c63a-1498-0201-e053-2995a90ad0cbb125c63a-14a6-0201-e053-2995a90ad0cb2020-10-08WarningsExact identifier
spl id: b125c63a-1498-0201-e053-2995a90ad0cb
spl set id: b125c63a-14a6-0201-e053-2995a90ad0cb

Reported adverse events (FAERS/openFDA)#

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