FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Specialty Graphics | YUYAO WANGCHENG DAILY COMMODITY CO., LTD.
Effective date
2022-10-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:51:13

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Use ​Decreases bacteria on hands

WARNINGS SECTION

Warnings For external use only

Flammable Keep away from fire or flame

Keep out of eyes In case of eye contact, immediately flush with water and get medical help.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions Squeeze onto hands and rub hands together briskly until dry.

Do Not Store Above 110°F

Non-staining, may discolor certain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Carbomer, Triethanolamine, Aloe Barbadensis Gel, Fragrance Glycerin, Propylene Glycol, Vitamin E.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HndsntrHndsntr

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN4
581660ethanol 0.62 ML/ML Topical GelSCD4
581660ethanol 62 % Topical GelSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73752-319-202024-01-30C16284748780-1c7ccaba7-2205-fd44-e053-dadaa90aa01bHand Sanitizer
73752-319-202022-10-27C16284748780-1c7ccaba7-2205-fd44-e053-dadaa90aa01bHand Sanitizer
73752-319-202022-07-29C16284748780-1c7ccaba7-2205-fd44-e053-dadaa90aa01bHand Sanitizer
73752-319-202021-07-23C16284748780-1c7ccaba7-2205-fd44-e053-dadaa90aa01bHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73752-319-20Hand Sanitizer50 mL in 1 BOTTLE, PLASTICGEL504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73752-319HAND SANITIZER (ETHYL ALCOHOL) GEL [SPECIALTY GRAPHICS]4Legacy NDC, 1 package rows20221029_2eb7aa23-747c-4b05-bb82-493c2dfb1cfd.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
73752-31973752-319-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT

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
f4b40b3a-19ff-4af6-93fd-5dba73affb642eb7aa23-747c-4b05-bb82-493c2dfb1cfd2022-10-27WarningsExact identifier
spl id: f4b40b3a-19ff-4af6-93fd-5dba73affb64
spl set id: 2eb7aa23-747c-4b05-bb82-493c2dfb1cfd

Reported adverse events (FAERS/openFDA)#

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