HAND SANITIZER

Manufacturer
Ningbo Lanzi Cosmetic Technology Co., Ltd
Effective date
2021-02-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:18

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place product on hands, rub 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

Hand sanitizer to reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable, keep away from fire and flame

For external use only

When using this product

do not use in or near eyes, in case of contact, rinse eyes thoroughly with water.

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

Place product on hands, rub until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Disodium EDTA, Tocopheryl acetate, Deionized Water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286291ethanol 68 % Topical SolutionPSN1
2286291ethanol 0.68 ML/ML Topical SolutionSCD1
2286291ethanol 68 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75613-016-012023-01-30C16284748780-1f386c64a-2352-0266-e053-dadaa90a7c1aHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75613-016-01HAND SANITIZER10 mL in 1 BOTTLELIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75613-016HAND SANITIZER (ETHYL ALCOHOL) LIQUID [NINGBO LANZI COSMETIC TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20210220_a5cf768d-c58f-4309-a563-cba7cb78d736.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75613-01675613-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dbaebd13-eea2-45b1-a59a-034087e5feeea5cf768d-c58f-4309-a563-cba7cb78d7362021-02-19WarningsExact identifier
spl id: dbaebd13-eea2-45b1-a59a-034087e5feee
spl set id: a5cf768d-c58f-4309-a563-cba7cb78d736

Reported adverse events (FAERS/openFDA)#

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