FDA.reportPublic FDA data

not have

Manufacturer
Guangzhou Yucaitang Cosmetics Co., Ltd.
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:47

Label at a glance#

Productnot have
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin.

Dosage and administration

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 106°F.(4I°C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 73.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

WARNINGS SECTION

Flammable.Keep away from fire or flame.For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and lasts.Keep out of reach for children.If swallowed,get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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 106°F.(4I°C)

May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER.GLYCERIN.CARBOMER.TRIETHANOLAMINE.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5 ml label5 ml label50 ml label50 ml label60 ml label60 ml label100 ml label100 ml label200 ml label200 ml label300 ml label300 ml label500 ml label500 ml label1 L label1 L label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286987ethanol 73 % Topical GelPSN1
2286987ethanol 0.73 ML/ML Topical GelSCD1
2286987ethanol 73 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75439-001-012022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-022022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-032022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-042022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-052022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-062022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-072022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER
75439-001-082022-01-28C16284748780-1d6a99b39-a599-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75439-001-01not have5 mL in 1 BAGGEL51
75439-001-02not have50 mL in 1 AMPULEGEL501
75439-001-03not have60 mL in 1 BOTTLEGEL601
75439-001-04not have100 mL in 1 BOTTLEGEL1001
75439-001-05not have200 mL in 1 BOTTLEGEL2001
75439-001-06not have300 mL in 1 BOTTLEGEL3001
75439-001-07not have500 mL in 1 BOTTLEGEL5001
75439-001-08not have1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75439-001NOT HAVE (HAND SANITIZER) GEL [GUANGZHOU YUCAITANG COSMETICS CO., LTD.]1Legacy NDC, 8 package rows20200506_a4df8b49-d86c-3703-e053-2995a90ad222.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
75439-00175439-001-01, 75439-001-02, 75439-001-03, 75439-001-04, 75439-001-05, 75439-001-06, 75439-001-07, 75439-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT

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
a3e321b5-1fc9-3f28-e053-2995a90a9627a4df8b49-d86c-3703-e053-2995a90ad2222020-04-22WarningsExact identifier
spl id: a3e321b5-1fc9-3f28-e053-2995a90a9627
spl set id: a4df8b49-d86c-3703-e053-2995a90ad222

Reported adverse events (FAERS/openFDA)#

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