Hand Sanitizing

Manufacturer: Ningbo Lizi Commodity Co., Ltd.
Effective date: 2020-08-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:00

Label at a glance#

ProductHand Sanitizing

Active ingredientALCOHOL

Label structure11 sections

Storage and handling

read all directions and warnings before using Store at room temperature 15℃ to 34℃ （59 ℉ to 86℉）with package closed. Avoid excessive heat above 40℃ (114℉）

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol .......... 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Premiun sanitizer to reduce 99.9% of most illness-causing germs and bacteria. Antiseptic for hands and skin. Sanitize and disinfect hands and skin when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

on open skin or puncture-type wounds.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation appears.

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.

direction

DOSAGE & ADMINISTRATION SECTION

Clean hands annd skin with by spraying on hands and skin and gently rubbing No need to rinse, let hands or skin dry

Other information

STORAGE AND HANDLING SECTION

read all directions and warnings before using

Store at room temperature 15℃ to 34℃ （59 ℉ to 86℉）with package closed.

Avoid excessive heat above 40℃ (114℉）

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Purified Water), Glycerinum

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286295	ethanol 75 % Topical Spray	PSN	1
2286295	ethanol 0.75 ML/ML Topical Spray	SCD	1
2286295	ethanol 75 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75329-1001-1	2022-01-28	C162847	48780-1	d6a99b39-4694-a426-e053-dadaa90af4c2	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75329-1001-1	Hand Sanitizing	5 mL in 1 BOTTLE, SPRAY	SPRAY	5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75329-1001	HAND SANITIZING (ALCOHOL) SPRAY [NINGBO LIZI COMMODITY CO., LTD.]	1	Legacy NDC, 1 package rows	20200828_a78d05dd-e256-4d94-8c51-af2bc1df11ea.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Hand Sanitizing
ALCOHOL
WATER
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75329-1001	75329-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	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
dd7ffcf7-3927-4eca-adb0-c0dc2d0d5a64			a78d05dd-e256-4d94-8c51-af2bc1df11ea	2020-08-26	Warnings	Exact identifier spl id: dd7ffcf7-3927-4eca-adb0-c0dc2d0d5a64 spl set id: a78d05dd-e256-4d94-8c51-af2bc1df11ea

Reported adverse events (FAERS/openFDA)#

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