Instant Hand Sanitizer

Manufacturer
Xi'an Explution Tech Co.,Ltd.
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:09

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

1.Pump enough amount of product in your palm to thoroughly spread on both hands. 2.Rub thoroughly over all surfaces of both hands. 3.Rub hands together briskly until dry.

Storage and handling

Store below 106°F.(41°C) May discolor certain fabrics or surface.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80%v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

USE

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

WARNINGS SECTION

For external use only.

Flammable.Keep away from heat or flame.

When using this product

OTC - WHEN USING SECTION

do not use on open skin Wounds.Keep out of eyes.ln.case of contact with eyes.rinse eyes thoroughly with water.

Use with caution if allergic to alcohoL.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation of rash appears and tasts.

Keep out of reach for children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed.get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

1.Pump enough amount of product in your palm to thoroughly spread on both hands.

2.Rub thoroughly over all surfaces of both hands.

3.Rub hands together briskly until dry.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store below 106°F.(41°C)

May discolor certain fabrics or surface.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

glycerin.hydrogen peroxide, purified water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml label60 ml label70 ml label70 ml label100 ml label100 ml label150 ml label150 ml label300 ml label300 ml label520 ml label520 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1041498ethanol 80 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75709-002-01Instant Hand Sanitizer60 mL in 1 BOTTLEGEL601
75709-002-02Instant Hand Sanitizer70 mL in 1 BOTTLEGEL701
75709-002-03Instant Hand Sanitizer100 mL in 1 BOTTLEGEL1001
75709-002-04Instant Hand Sanitizer150 mL in 1 BOTTLEGEL1501
75709-002-05Instant Hand Sanitizer300 mL in 1 BOTTLEGEL3001
75709-002-06Instant Hand Sanitizer520 mL in 1 BOTTLEGEL5201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75709-002INSTANT HAND SANITIZER GEL [XI'AN EXPLUTION TECH CO.,LTD.]1Legacy NDC, 6 package rows20200501_a479cf19-1429-3111-e053-2995a90a6ce8.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
75709-00275709-002-01, 75709-002-02, 75709-002-03, 75709-002-04, 75709-002-05, 75709-002-06

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 · 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
a478f654-976d-5293-e053-2995a90acad4a479cf19-1429-3111-e053-2995a90a6ce82020-04-29WarningsExact identifier
spl id: a478f654-976d-5293-e053-2995a90acad4
spl set id: a479cf19-1429-3111-e053-2995a90a6ce8

Reported adverse events (FAERS/openFDA)#

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