HAND SANITIZER

Manufacturer: Fortress Expert Co., Ltd
Effective date: 2020-06-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:08

Label at a glance#

ProductHAND SANITIZER

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Helps reduce bacteria that potentially can cause disease Helps prevent cross contamination by hand contact Recommended for repeated use

Dosage and administration

Wet hands thoroughly with product and and rub completely covering hands Allow to dry without wiping Children under the age of 6 should use with adult supervision Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75.05%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Helps reduce bacteria that potentially can cause disease

Helps prevent cross contamination by hand contact

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire, heat,or flame

Do not use near eyes

In case of eye contact flush with water for 15 minutes

if irritation persists stop use of product and get medical attention

Keep out of reach of children.

In case of accidental ingestion seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and and rub completely covering hands

Allow to dry without wiping

Children under the age of 6 should use with adult

supervision

Not recommended for infants

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-40 Hydrogenated Castor Oil, Carbomer,

Fragrance (Parfum), Triethanolamine, Triisopropanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785946200060

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2367754	ethanol 75.1 % Topical Gel	PSN	1
2367754	ethanol 0.751 ML/ML Topical Gel	SCD	1
2367754	ethanol 75.1 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73549-005-01	2022-01-28	C162847	48780-1	d6a99b39-737c-a426-e053-dadaa90af4c2	HAND SANITIZER
73549-005-02	2022-01-28	C162847	48780-1	d6a99b39-737c-a426-e053-dadaa90af4c2	HAND SANITIZER
73549-005-03	2022-01-28	C162847	48780-1	d6a99b39-737c-a426-e053-dadaa90af4c2	HAND SANITIZER
73549-005-04	2022-01-28	C162847	48780-1	d6a99b39-737c-a426-e053-dadaa90af4c2	HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73549-005-01	HAND SANITIZER	60 mL in 1 BOTTLE	GEL	60	1
73549-005-02	HAND SANITIZER	946.35 mL in 1 BOTTLE	GEL	946.35	1
73549-005-03	HAND SANITIZER	2000 mL in 1 BOTTLE	GEL	2000	1
73549-005-04	HAND SANITIZER	3785.4 mL in 1 BOTTLE	GEL	3785.4	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73549-005	HAND SANITIZER GEL [FORTRESS EXPERT CO., LTD]	1	Legacy NDC, 4 package rows	20200611_a7b72113-d717-5793-e053-2995a90af570.zip

Products#

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

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

HAND SANITIZER
ALCOHOL
FRAGRANCE LAVENDER & CHIA F-153480
TROLAMINE
POLYOXYL 40 HYDROGENATED CASTOR OIL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
TRIISOPROPANOLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73549-005	73549-005-01, 73549-005-02, 73549-005-03, 73549-005-04

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
ALCOHOL	3K9958V90M	ACTIB
FRAGRANCE LAVENDER & CHIA F-153480	SXS9CO2TZK	IACT
TROLAMINE	9O3K93S3TK	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
TRIISOPROPANOLAMINE	W9EN9DLM98	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
a7b72113-d718-5793-e053-2995a90af570			a7b72113-d717-5793-e053-2995a90af570	2020-06-10	Warnings	Exact identifier spl id: a7b72113-d718-5793-e053-2995a90af570 spl set id: a7b72113-d717-5793-e053-2995a90af570

Reported adverse events (FAERS/openFDA)#

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