Instant Hand Sanitizer

Manufacturer
Venus Skin & Hair Laboratory Ltd.
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:43

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Do not place this product in high temperature or direct sunlight.

INACTIVE INGREDIENT SECTION

water

propylene glycol

glycerin

carbomer triethanolamine

INDICATIONS & USAGE SECTION

when you wash your hands,squeeze some of the gel into your hands and rub it with your hand unitl are dry.

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

Do not place this product in high temperature or direct sunlight.keep out of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2361058ethanol 68.4 % Topical GelPSN1
2361058ethanol 0.684 ML/ML Topical GelSCD1
2361058ethanol 68.4 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54708-002-012022-01-28C16284748780-1d6a99b39-bdf4-a426-e053-dadaa90af4c2a4041d3f-6540-34f1-e053-2a95a90af1dd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54708-002-01Instant Hand Sanitizer100 mL in 1 BOTTLEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54708-002INSTANT HAND SANITIZER (HAND SANITIZER) GEL [VENUS SKIN & HAIR LABORATORY LTD.]1Legacy NDC, 1 package rows20200424_a4041d3f-6540-34f1-e053-2a95a90af1dd.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
54708-00254708-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
a4040898-ca17-8758-e053-2995a90aec3ea4041d3f-6540-34f1-e053-2a95a90af1dd2020-04-24WarningsExact identifier
spl id: a4040898-ca17-8758-e053-2995a90aec3e
spl set id: a4041d3f-6540-34f1-e053-2a95a90af1dd

Reported adverse events (FAERS/openFDA)#

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