FDA.reportPublic FDA data

Waterless Hand Sanitizer Gel

Manufacturer
Ugel Pharm Tech (Shanghai) Co., Ltd.
Effective date
2020-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:16

Label at a glance#

ProductWaterless Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store in a cool and dry place

INACTIVE INGREDIENT SECTION

Water, Glycerol, Sodium Hyaluronate, Carbomer, TEOA, Essence

INDICATIONS & USAGE SECTION

Use 2 - 3ML to Moisten Hands and Rub 15 Seconds till to Dry

OTC - ACTIVE INGREDIENT SECTION

Alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

External Use Only, Keep out of Reach of Children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
55262-002-012022-01-28C16284748780-1d6a99b39-c16d-a426-e053-dadaa90af4c2a637b441-bf14-f097-e053-2a95a90a7902

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55262-002-01Waterless Hand Sanitizer Gel500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55262-002WATERLESS HAND SANITIZER GEL (WATERLESS HAND SANITIZER) GEL [UGEL PHARM TECH (SHANGHAI) CO., LTD.]1Legacy NDC, 1 package rows20200522_a637b441-bf14-f097-e053-2a95a90a7902.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
55262-00255262-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
METHYL BENZOATE6618K1VJ9TIACT
GLYCERINPDC6A3C0OXIACT

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
a637b441-bf15-f097-e053-2a95a90a7902a637b441-bf14-f097-e053-2a95a90a79022020-05-22WarningsExact identifier
spl id: a637b441-bf15-f097-e053-2a95a90a7902
spl set id: a637b441-bf14-f097-e053-2a95a90a7902

Reported adverse events (FAERS/openFDA)#

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