FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
LOTUS ARTS CRAFTS LIMITED
Effective date
2020-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:15

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Store below 105° F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use for hand

INDICATIONS & USAGE SECTION

washing to decrease bacteria on the skin ,only when water is not available

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

Do not get into eyes. If contact occurs ,rinse eyes thoroughly with water

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Imitation and redness develop.
Keep out of reach of children.
If swallowed ,get medical help for contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

Store below 105° F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua(water) ,Glycerin, Carbomer, Propylene glycol, Triethanolamine ,Aloe Barbadensis Leaf Extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130067722289892GTIN-13: 0067722289892
EAN-13: 0067722289892
GTIN-12: 067722289892
UPC-A: 067722289892
GTIN storage (14 digits): 00067722289892		package.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78294-001-012022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer
78294-001-022022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer
78294-001-032022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer
78294-001-042022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer
78294-001-052022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer
78294-001-062022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer
78294-001-072022-01-28C16284748780-1d6a99b39-8cfe-a426-e053-dadaa90af4c2hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78294-001-01Instant Hand Sanitizer30 mL in 1 BOTTLEGEL301
78294-001-02Instant Hand Sanitizer60 mL in 1 BOTTLEGEL601
78294-001-03Instant Hand Sanitizer100 mL in 1 BOTTLEGEL1001
78294-001-04Instant Hand Sanitizer250 mL in 1 BOTTLEGEL2501
78294-001-05Instant Hand Sanitizer300 mL in 1 BOTTLEGEL3001
78294-001-06Instant Hand Sanitizer500 mL in 1 BOTTLEGEL5001
78294-001-07Instant Hand Sanitizer1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78294-001INSTANT HAND SANITIZER (ALCOHOL) GEL [LOTUS ARTS CRAFTS LIMITED]1Legacy NDC, 7 package rows20200522_a6378a16-f5ff-55a9-e053-2995a90a7377.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
78294-00178294-001-01, 78294-001-02, 78294-001-03, 78294-001-04, 78294-001-05, 78294-001-06, 78294-001-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
a6379805-cda3-13ae-e053-2995a90a7d30a6378a16-f5ff-55a9-e053-2995a90a73772020-05-22WarningsExact identifier
spl id: a6379805-cda3-13ae-e053-2995a90a7d30
spl set id: a6378a16-f5ff-55a9-e053-2995a90a7377

Reported adverse events (FAERS/openFDA)#

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