FDA.reportPublic FDA data

ANTIBACTERIAL HAND SANITIZER

Manufacturer
ASC Marketing Ltd.
Effective date
2020-11-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:22

Label at a glance#

ProductANTIBACTERIAL HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

for handwashing to decrease bacteria on the skin. recommended for repeated use.

Dosage and administration

wet hands thoroughly with product. briskly rub hands together until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Do not use in eyes.
  • Discontinue use if irritation and redness develop.
  • Flammable, keep away from fire or flame.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

If pregnant or breast-feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product.
  • briskly rub hands together until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aloe Barbadensis Leaf Juice, Maltodextrin, Triethanolamine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73145-005-012025-01-30C16284748780-12cef2736-7576-d83d-e063-dadaa90ab31fASC ANTIBACTERIAL HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73145-005-01ANTIBACTERIAL HAND SANITIZER15 mL in 1 BOTTLE, PLASTICGEL151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73145-005ANTIBACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [ASC MARKETING LTD.]1Legacy NDC, 1 package rows20201111_b3cb9eac-5227-40cc-e053-2a95a90aec0d.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73145-00573145-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MALTODEXTRIN7CVR7L4A2DIACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
b3caa9c8-67e4-c737-e053-2a95a90a8970b3cb9eac-5227-40cc-e053-2a95a90aec0d2020-11-10WarningsExact identifier
spl id: b3caa9c8-67e4-c737-e053-2a95a90a8970
spl set id: b3cb9eac-5227-40cc-e053-2a95a90aec0d

Reported adverse events (FAERS/openFDA)#

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