FDA.reportPublic FDA data

Antibacterial Hand Sanitizer

Manufacturer
Huizhou Baozi Biotechnology Co., Ltd.
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:14

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria on skin

Dosage and administration

Directions: Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry Children under 6 years of age should be supervised when using this product

Storage and handling

Store below 106F(41C).May discolor certain fabnics orsurfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fre or fiame
For external use only.

OTC - DO NOT USE SECTION

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

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

stop use and ask a doctor if imitation 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

Directions: Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry

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

Other information

STORAGE AND HANDLING SECTION

Store below 106F(41C).May discolor certain fabnics orsurfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol,Aloe Barbadensis Leat Juice, Caprylyl Glycol， Glycerin, isopropyl Miristate, Acrylates/C10-30 Alky Acrylate Crosspolymer, Amnomethyl Propanol, Fragrance(parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74881-008-05 3800mL74881-008-05 3800mL74881-008-01 59ml74881-008-01 59ml74881-008-02 118ml74881-008-02 118ml74881-008-03 248ml74881-008-03 248ml74881-008-04 500ml74881-008-04 500ml

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
74881-008-012022-01-28C16284748780-1d6a99b39-ada4-a426-e053-dadaa90af4c2008 Antibacterial Hand Sanitizer
74881-008-022022-01-28C16284748780-1d6a99b39-ada4-a426-e053-dadaa90af4c2008 Antibacterial Hand Sanitizer
74881-008-032022-01-28C16284748780-1d6a99b39-ada4-a426-e053-dadaa90af4c2008 Antibacterial Hand Sanitizer
74881-008-042022-01-28C16284748780-1d6a99b39-ada4-a426-e053-dadaa90af4c2008 Antibacterial Hand Sanitizer
74881-008-052022-01-28C16284748780-1d6a99b39-ada4-a426-e053-dadaa90af4c2008 Antibacterial Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74881-008-01Antibacterial Hand Sanitizer59 mL in 1 BOTTLEGEL591
74881-008-02Antibacterial Hand Sanitizer118 mL in 1 BOTTLEGEL1181
74881-008-03Antibacterial Hand Sanitizer248 mL in 1 BOTTLEGEL2481
74881-008-04Antibacterial Hand Sanitizer500 mL in 1 BOTTLEGEL5001
74881-008-05Antibacterial Hand Sanitizer3800 mL in 1 BOTTLEGEL38001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74881-008ANTIBACTERIAL HAND SANITIZER GEL [HUIZHOU BAOZI BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 5 package rows20200820_ad390eac-ac54-797d-e053-2995a90a5333.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
74881-00874881-008-01, 74881-008-02, 74881-008-03, 74881-008-04, 74881-008-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
CAPRYLYL GLYCOL00YIU5438UIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ISOPROPYL ALCOHOLND2M416302IACT

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
ad38aef7-6384-3a83-e053-2995a90a4249ad390eac-ac54-797d-e053-2995a90a53332020-08-19WarningsExact identifier
spl id: ad38aef7-6384-3a83-e053-2995a90a4249
spl set id: ad390eac-ac54-797d-e053-2995a90a5333

Reported adverse events (FAERS/openFDA)#

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