Instant Hand Sanitizer

Manufacturer
JIANGSU AIMEILI COSMETIC CO.,LTD
Effective date
2024-01-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:06:39

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hands thoughly with product and rub until dry without wiping for children under 6,use only under adult supervision not recommended for infants

Storage and handling

do not store above 105℉ may discolor some fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ethanol 75% (v/v) Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

recommended for repeated use

use without water

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame

discontinue if skin becomes irritated and ask a doctor

keep out of reach of children, in case of accodental igestion,seek prefessional assistance or contact a poison control center immediately

OTC - DO NOT USE SECTION

do not inhale or ingest

do not use on open skin wounds.

when using this product

OTC - WHEN USING SECTION

keep out of eyes.In case of contacting with eyes,flush thoroughly with water.

do not inhale or ingest

do not use on open skin wounds

OTC - STOP USE SECTION

discontine of skin becomes irritated and ask a doctor.

Keep out of reach of children,in case of accidental ingestion,seek professional assistance or contact a poison control center immediately

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. in case of accidental ingestion,seek professional assistance or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoughly with product and rub until dry without wiping

for children under 6,use only under adult supervision

not recommended for infants

Other information

STORAGE AND HANDLING SECTION

do not store above 105℉

may discolor some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua,Aloe extract, triethanolamine,glycerin,carbomer,vitamin E

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77573-002-01Instant Hand Sanitizer50 mL in 1 BOTTLEGEL502
77573-002-02Instant Hand Sanitizer100 mL in 1 BOTTLEGEL1002
77573-002-03Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77573-002INSTANT HAND SANITIZER (ALCOHOL) GEL [JIANGSU AIMEILI COSMETIC CO.,LTD]2Legacy NDC, 3 package rows20240105_a98197f6-1b3f-1a6c-e053-2995a90a26cd.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77573-00277573-002-01, 77573-002-02, 77573-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
0e2d1926-f1f2-8462-e063-6394a90aa350a98197f6-1b3f-1a6c-e053-2995a90a26cd2024-01-05WarningsExact identifier
spl id: 0e2d1926-f1f2-8462-e063-6394a90aa350
spl set id: a98197f6-1b3f-1a6c-e053-2995a90a26cd

Reported adverse events (FAERS/openFDA)#

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