Hand Sanitizer Gel

Manufacturer: Hangzhou Huiji Biotechnology Co., Ltd.
Effective date: 2022-02-24
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:48:25

Label at a glance#

ProductHand Sanitizer Gel

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Squeeze small amount in your palm and briskly rub hands together, and allow to air dry. For children under 6, use with adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria
on the skin.

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire or
flame. For external use only. Keep
out of reach of children. Keep away
from eyes. Do not inhale or ingest.
Stop use and ask doctor if irritation
or redness develops.

keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

Squeeze small amount in your
palm and briskly rub hands
together, and allow to air dry.
For children under 6, use with adult
supervision. Not recommended for
infants.

Other Information

SPL UNCLASSIFIED SECTION

Store below 110 F (43 C). May
discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients Water,
Glycerin, Aloe barbadensis leaf extract,
Carbomer.Tocopheryl Acetate,
Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	2
581660	ethanol 0.62 ML/ML Topical Gel	SCD	2
581660	ethanol 62 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73788-101-01	2025-01-30	C162847	48780-1	d6a99b39-f1ac-a426-e053-dadaa90af4c2	73788-101 Hand Sanitizer Gel
73788-101-01	2022-02-24	C162847	48780-1	d6a99b39-f1ac-a426-e053-dadaa90af4c2	73788-101 Hand Sanitizer Gel
73788-101-01	2022-01-28	C162847	48780-1	d6a99b39-f1ac-a426-e053-dadaa90af4c2	73788-101 Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73788-101-01	Hand Sanitizer Gel	237 mL in 1 BOTTLE	GEL	237		2
73788-101-01	Hand Sanitizer Gel	24 in 1 CARTON	GEL	24		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73788-101	HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [HANGZHOU HUIJI BIOTECHNOLOGY CO., LTD.]	2	Legacy NDC, 2 package rows	20220224_a4aa48ca-9edb-665a-e053-2995a90a81c3.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Hand Sanitizer Gel
Ethyl Alcohol
WATER
GLYCERIN
ALOE VERA LEAF
TROLAMINE
CARBOMER 934
.ALPHA.-TOCOPHEROL ACETATE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73788-101	73788-101-01

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
ALOE VERA LEAF	ZY81Z83H0X	IACT
TROLAMINE	9O3K93S3TK	IACT
CARBOMER 934	Z135WT9208	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

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
d8bf87fe-2d1d-cceb-e053-2a95a90aea54			a4aa48ca-9edb-665a-e053-2995a90a81c3	2022-02-24	Warnings	Exact identifier spl id: d8bf87fe-2d1d-cceb-e053-2a95a90aea54 spl set id: a4aa48ca-9edb-665a-e053-2995a90a81c3

Reported adverse events (FAERS/openFDA)#

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