FDA.reportPublic FDA data

STAR WATERLESS HAND SANITIZERGEL

Manufacturer
Shenzhen City Yaoxing Industry Corp., Ltd
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:10

Label at a glance#

ProductSTAR WATERLESS HAND SANITIZERGEL
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

store in a cool place

INACTIVE INGREDIENT SECTION

TRIETHANOLAMINE

TRICLOSAN

PROPHYLENE GLYCOL

WATER

Aloe extract

INDICATIONS & USAGE SECTION

Rub your hand thoroughly with hand sanitizer and let it air dry.

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

Don't direct spray on eye. In case of contact with eyes,rinse imnediately with plenty of water and seek medicaI attention.

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
52688-001-012022-01-28C16284748780-1d6a99b39-f312-a426-e053-dadaa90af4c2a5a6eb63-bd8c-0c1b-e053-2a95a90a376c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52688-001-01STAR WATERLESS HAND SANITIZERGEL500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52688-001STAR WATERLESS HAND SANITIZERGEL (HAND SANITIZER) GEL [SHENZHEN CITY YAOXING INDUSTRY CORP., LTD]1Legacy NDC, 1 package rows20200515_a5a6eb63-bd8c-0c1b-e053-2a95a90a376c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52688-00152688-001-01

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
ALOEV5VD430YW9IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TRICLOSAN4NM5039Y5XIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT

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
a5a6eb63-bd8d-0c1b-e053-2a95a90a376ca5a6eb63-bd8c-0c1b-e053-2a95a90a376c2020-05-14WarningsExact identifier
spl id: a5a6eb63-bd8d-0c1b-e053-2a95a90a376c
spl set id: a5a6eb63-bd8c-0c1b-e053-2a95a90a376c

Reported adverse events (FAERS/openFDA)#

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