Hand Sanitizer

Manufacturer
XIAMEN HONGSHIXIN TECHNOLOGY CO.,LTD
Effective date
2020-08-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:38

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

store below 105°F.

INACTIVE INGREDIENT SECTION

WATER

CARBOMER

TRIETHANOLAMINE

INDICATIONS & USAGE SECTION

Take an appropriate amount (2-3 ml) of product to moisten your hands and rub for 15 seconds until the liquid covers your hands, wait for drying and do not wash with water.

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

For external use only.Flammable, keep away from fire or flame.

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
96175-001-012022-01-28C16284748780-1d6a99b39-c5fa-a426-e053-dadaa90af4c2abefed03-5755-7794-e053-2a95a90af41b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
96175-001-01Hand Sanitizer236 mL in 1 BOTTLEGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
96175-001HAND SANITIZER GEL [XIAMEN HONGSHIXIN TECHNOLOGY CO.,LTD]1Legacy NDC, 1 package rows20200804_abefed03-5755-7794-e053-2a95a90af41b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
96175-00196175-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
abefed03-5756-7794-e053-2a95a90af41babefed03-5755-7794-e053-2a95a90af41b2020-08-02WarningsExact identifier
spl id: abefed03-5756-7794-e053-2a95a90af41b
spl set id: abefed03-5755-7794-e053-2a95a90af41b

Reported adverse events (FAERS/openFDA)#

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