Antibacterial Hand Sanitizer

Manufacturer: ASC Marketing LTD
Effective date: 2023-12-01
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:03:09

Label at a glance#

ProductAntibacterial Hand Sanitizer

Active ingredientALCOHOL

Label structure8 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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

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, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Fragrance

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2

Package Labeling:73145-003-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73145-003-01	Antibacterial Hand Sanitizer	30 mL in 1 BOTTLE	GEL	30	3
73145-003-02	Antibacterial Hand Sanitizer	60 mL in 1 BOTTLE	GEL	60	3
73145-003-03	Antibacterial Hand Sanitizer	15 mL in 1 BOTTLE	GEL	15	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73145-003	ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [ASC MARKETING LTD]	3	Current NDC, Legacy NDC, 3 package rows	20231202_b56d6034-cac2-a9e2-e053-2a95a90aebf0.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Antibacterial Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
PROPYLENE GLYCOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73145-003	73145-003-01, 73145-003-02, 73145-003-03

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Antibacterial Hand Sanitizer	ALCOHOL	ASC Marketing LTD	b56d6034-cac2-a9e2-e053-2a95a90aebf0	2023-12-01	Warnings	Exact identifier ndc (package): 73145-003-01 ndc (package): 73145-003-02 ndc (package): 73145-003-03 ndc (product): 73145-003 ndc11 (package): 73145000302 ndc11 (package): 73145000301 ndc11 (package): 73145000303 spl id: 0b6e0023-a810-dcd8-e063-6394a90a52ae spl set id: b56d6034-cac2-a9e2-e053-2a95a90aebf0

Reported adverse events (FAERS/openFDA)#

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