FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Guangzhou Taisheng Biotechnology Co., Ltd.
Effective date
2020-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:11

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all .surfaces. Rub hands together until dry. Supervise children under6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C(59-86F) Avoid frezzing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

75%Alcohol

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sa nitiazer to help reduce bacteria that potentially can cause d isease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

l.Do not mix with other hand sanitizers
2.Keep out of reaching of children
3.This product is for externa I use, please do not eat it
4.Avoid contact with eyes
5.Keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

/

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all .surfaces. Rub hands together until dry. Supervise children under6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C(59-86F)
Avoid frezzing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Carbomer, Triethanolamine, Glycerol, Aloe vera

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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
79603-001-012021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-022021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-032021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-042021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-052021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-062021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-072021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-082021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-092021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER
79603-001-102021-07-23C16284748780-1c7ccaba7-2ab7-fd44-e053-dadaa90aa01bHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79603-001-01HAND SANITIZER30 mL in 1 BOTTLEGEL301
79603-001-02HAND SANITIZER50 mL in 1 BOTTLEGEL501
79603-001-03HAND SANITIZER60 mL in 1 BOTTLEGEL601
79603-001-04HAND SANITIZER100 mL in 1 BOTTLEGEL1001
79603-001-05HAND SANITIZER300 mL in 1 BOTTLEGEL3001
79603-001-06HAND SANITIZER500 mL in 1 BOTTLEGEL5001
79603-001-07HAND SANITIZER750 mL in 1 BOTTLEGEL7501
79603-001-08HAND SANITIZER1000 mL in 1 BOTTLEGEL10001
79603-001-09HAND SANITIZER2000 mL in 1 BOTTLEGEL20001
79603-001-10HAND SANITIZER5000 mL in 1 BOTTLEGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79603-001HAND SANITIZER GEL [GUANGZHOU TAISHENG BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 10 package rows20200714_aa4e20ce-dde3-3102-e053-2995a90a3e8f.zip

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
79603-00179603-001-01, 79603-001-02, 79603-001-03, 79603-001-04, 79603-001-05, 79603-001-06, 79603-001-07, 79603-001-08, 79603-001-09, 79603-001-10

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
ALOE VERA LEAFZY81Z83H0XIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
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
aa4e03b3-a372-6418-e053-2a95a90a9c65aa4e20ce-dde3-3102-e053-2995a90a3e8f2020-07-13WarningsExact identifier
spl id: aa4e03b3-a372-6418-e053-2a95a90a9c65
spl set id: aa4e20ce-dde3-3102-e053-2995a90a3e8f

Reported adverse events (FAERS/openFDA)#

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