HAND SANITIZER

Manufacturer: Ningbo Lanzi Cosmetic Technology Co., Ltd
Effective date: 2020-05-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:14:16

Label at a glance#

ProductHAND SANITIZER

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing

Warnings

WARNINGS SECTION

For external use only.

Flammable.Keep away from heat and flame.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin.

Stop use and ask a doctor if

rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub hands together briskly until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin,Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium Edta, Tocopheryl Acetate, Deionized Water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1037039	ethanol 68 % Topical Gel	PSN	1
1037039	ethanol 0.68 ML/ML Topical Gel	SCD	1
1037039	ethanol 68 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75613-008-01	2022-01-28	C162847	48780-1	d6a99b39-f406-a426-e053-dadaa90af4c2	HAND SANITIZER
75613-008-02	2022-01-28	C162847	48780-1	d6a99b39-f406-a426-e053-dadaa90af4c2	HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75613-008-01	HAND SANITIZER	20 mL in 1 BOTTLE	GEL	20		1
75613-008-02	HAND SANITIZER	10 mL in 1 BOTTLE	GEL	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75613-008	HAND SANITIZER (ALCOHOL) GEL [NINGBO LANZI COSMETIC TECHNOLOGY CO., LTD]	1	Legacy NDC, 2 package rows	20200522_b03f458b-7676-4157-85b2-9c97fe63ebc4.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
WATER
PROPYLENE GLYCOL
EDETATE DISODIUM
TROLAMINE
.ALPHA.-TOCOPHEROL ACETATE, D-
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75613-008	75613-008-01, 75613-008-02

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
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
TROLAMINE	9O3K93S3TK	IACT
.ALPHA.-TOCOPHEROL ACETATE, D-	A7E6112E4N	IACT
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
663c3642-06c5-45c0-a0e7-4d9e36c7c59b			b03f458b-7676-4157-85b2-9c97fe63ebc4	2020-05-22	Warnings	Exact identifier spl id: 663c3642-06c5-45c0-a0e7-4d9e36c7c59b spl set id: b03f458b-7676-4157-85b2-9c97fe63ebc4

Reported adverse events (FAERS/openFDA)#

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