Instant Hand Sanitizer

Manufacturer
Venus Skin & Hair Laboratory Ltd. | A03 Lab of BTS
Effective date
2020-05-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:45

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Take 2ml of this product and directly apply it to the skin of the hand. Leave for 1 minute and let it air dry. No need to wash with water. Repeated use may cause a slight sticky feeling, can rinse with water.

Storage and handling

Store in an environment below 50℃. Please cap the bottle after use to avoid volatilization.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial.

Use

INDICATIONS & USAGE SECTION

Uses for handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

It is flammable and must kept away from fire.
For external use, do not take orally.

Do not use

OTC - DO NOT USE SECTION

Avoid contact with eyes, if this occurs, rinse immediately with plenty of water.
Alcohol allergy should be used with caution.

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes or wound.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Take 2ml of this product and directly apply it to the skin of the hand.
Leave for 1 minute and let it air dry.
No need to wash with water.
Repeated use may cause a slight sticky feeling, can rinse with water.

Other information

STORAGE AND HANDLING SECTION

Store in an environment below 50℃.
Please cap the bottle after use to avoid volatilization.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54708-011-012022-01-28C16284748780-1d6a99b39-f374-a426-e053-dadaa90af4c2Venus, Hand Sanitizer, 70% Ethyl Alcohol, Liquid, 100mL, Bottle-Plastic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54708-011-01Instant Hand Sanitizer100 mL in 1 BOTTLE, PLASTICLIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54708-011INSTANT HAND SANITIZER LIQUID [VENUS SKIN & HAIR LABORATORY LTD.]1Legacy NDC, 1 package rows20200520_a5f1d511-39f0-1e4f-e053-2a95a90aab08.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54708-01154708-011-01

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
a5f1d511-39f1-1e4f-e053-2a95a90aab08a5f1d511-39f0-1e4f-e053-2a95a90aab082020-05-19WarningsExact identifier
spl id: a5f1d511-39f1-1e4f-e053-2a95a90aab08
spl set id: a5f1d511-39f0-1e4f-e053-2a95a90aab08

Reported adverse events (FAERS/openFDA)#

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