Hand Sanitizer

Manufacturer: Huizhou Baozi Biotechnology Co., Ltd.
Effective date: 2021-01-06
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:36:33

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

Use: Hand sanitizer to help, reduce bacteria on skin

Dosage and administration

Directions: Put enough product n your palm to cover hands and rub hands together brady until dry Children 6 years of age should be supervised when using

Storage and handling

Other information: Store at room temperature Keep container tightly closed in a dry and well-ventilated place Avoid storage under direct sunlight Keep out of reach of children

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Use: Hand sanitizer to help, reduce bacteria on skin

Warnings

WARNINGS SECTION

Warnings. Flammable. Keep away from fire or flame For extend use or When using this product do not use in or near the eyes. in case of contact, rinse eyes thoroughly with water. stop use and ask a doctor if imitation or rash appears and lasts. Keep out of reach of children. I swallowed, get medical help or contact a Poison Control Center immediately

OTC - DO NOT USE SECTION

When using this product do not use in or near the eyes

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes.

OTC - STOP USE SECTION

stop use and ask a doctor if imitation or rash appears and lasts.

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 immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Put enough product n your palm to cover hands and rub hands together brady until dry

Children 6 years of age should be supervised when using

Other information

STORAGE AND HANDLING SECTION

Other information: Store at room temperature

Keep container tightly closed in a dry and well-ventilated place

Avoid storage under direct sunlight

Keep out of reach of children

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Isopropyl Alcohol , Aloe Barbadensis Leaf Juice,

Caprylyl Glycol, Glycerin, Isopropyl Miristate, Acrylates/C10-30 Alky Acrylate Cross polymer,

Aminomethyl Propanol, Fragrance(Parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74881-005-01 150ml 1

74881-005-02 150ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286295	ethanol 75 % Topical Spray	PSN	2
2286295	ethanol 0.75 ML/ML Topical Spray	SCD	2
2286295	ethanol 75 % Topical Spray	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74881-005-01	2022-07-29	C162847	48780-1	e4f33bdf-ab00-d8a0-e053-dadaa90a6e4e	74881-005 Hand Sanitizer
74881-005-02	2022-07-29	C162847	48780-1	e4f33bdf-ab00-d8a0-e053-dadaa90a6e4e	74881-005 Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74881-005-01	Hand Sanitizer	150 mL in 1 BOTTLE, SPRAY	SPRAY	150		2
74881-005-02	Hand Sanitizer	150 mL in 1 BOTTLE, SPRAY	SPRAY	150		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74881-005	HAND SANITIZER (HAND SANITIZER SPRAY) SPRAY [HUIZHOU BAOZI BIOTECHNOLOGY CO., LTD.]	2	Legacy NDC, 2 package rows	20210107_a8bfe8b7-29ce-108d-e053-2995a90ac07c.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Hand Sanitizer
Hand Sanitizer Spray
CAPRYLYL GLYCOL
ISOPROPYL MYRISTATE
GLYCERIN
ALOE VERA LEAF
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
WATER
ISOPROPYL ALCOHOL
ALCOHOL
1-AMINOBUTAN-2-OL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74881-005	74881-005-01, 74881-005-02

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
CAPRYLYL GLYCOL	00YIU5438U	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	IACT
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
ALCOHOL	3K9958V90M	ACTIB
1-AMINOBUTAN-2-OL	19453GN3YQ	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
b8463e0e-fdc6-409f-e053-2995a90a154f			a8bfe8b7-29ce-108d-e053-2995a90ac07c	2021-01-06	Warnings	Exact identifier spl id: b8463e0e-fdc6-409f-e053-2995a90a154f spl set id: a8bfe8b7-29ce-108d-e053-2995a90ac07c

Reported adverse events (FAERS/openFDA)#

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