FARMACY ANTISEPTIC HAND SANITIZER

Manufacturer: GuStar Co Ltd
Effective date: 2020-04-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:06:42

Label at a glance#

ProductFARMACY ANTISEPTIC HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Uses Hand sanitizer to help reduce bacteria on skin only when water and soap is not available

Dosage and administration

Directions • Wet hands throughly with product and rub hands together until dry • Supervise children under 6 years of age when using.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ETHANOL 70% v/v

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Glycerin, Carbomer, Dipropylene Glycol, Isopropylene Myristate, Triethanolamine, Citrus Paradisi (Grapefruit) Seed Extract, Aloe Barbadensis Leaf Juice Powder

PURPOSE

OTC - PURPOSE SECTION

Purpose: ANTISEPTIC

WARNINGS

WARNINGS SECTION

Warnings

For external use only. Flammable. Keep away from heat and flame
--------------------------------------------------------------------------------------------------------
When using this product
keep out of eyes, ears, and mouth.
if contact occurs, rinse eyes thoroughly with water
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor
if irritation or rash occurs.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Uses

Hand sanitizer to help reduce bacteria on skin only when water and soap is not available

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

• Wet hands throughly with product and rub hands together until dry
• Supervise children under 6 years of age when using.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of container

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73819-0005-1	2022-07-29	C162847	48780-1	e4f33bdf-ab4c-d8a0-e053-dadaa90a6e4e	7524e203-e162-42b1-8f6b-0c3a2268a31b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73819-0005-1	FARMACY ANTISEPTIC HAND SANITIZER	60 mL in 1 CONTAINER	GEL	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73819-0005	FARMACY ANTISEPTIC HAND SANITIZER (ALCOHOL) GEL [GUSTAR CO LTD]	1	Legacy NDC, 1 package rows	20200418_7524e203-e162-42b1-8f6b-0c3a2268a31b.zip

Products#

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

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

FARMACY ANTISEPTIC HAND SANITIZER
ALCOHOL
Water
Glycerin
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
Dipropylene Glycol
ISOPROPYL MYRISTATE
Trolamine
CITRUS PARADISI SEED
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73819-0005	73819-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
Glycerin	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
Dipropylene Glycol	E107L85C40	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
Trolamine	9O3K93S3TK	IACT
CITRUS PARADISI SEED	12F08874Y7	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT

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
1b3c5414-38a6-40b7-877b-b73faa32da1f			7524e203-e162-42b1-8f6b-0c3a2268a31b	2020-04-18	Warnings	Exact identifier spl id: 1b3c5414-38a6-40b7-877b-b73faa32da1f spl set id: 7524e203-e162-42b1-8f6b-0c3a2268a31b

Reported adverse events (FAERS/openFDA)#

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