HAND SANITIZER

Manufacturer
Ningbo Lanzi Cosmetic Technology Co., Ltd
Effective date
2020-06-23
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 23:18:35

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 62%

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizing to reduce bacteria on skin.

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire and flame.

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, Fragrance, Disodium edtatocopheryl acetate, Deionized Water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN10
581660ethanol 0.62 ML/ML Topical GelSCD10
581660ethanol 62 % Topical GelSY10

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75613-005-012022-01-28C16284748780-1d6a99b39-8fa1-a426-e053-dadaa90af4c2HAND SANITIZER
75613-005-022022-01-28C16284748780-1d6a99b39-8fa1-a426-e053-dadaa90af4c2HAND SANITIZER
75613-005-032022-01-28C16284748780-1d6a99b39-8fa1-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75613-005-01HAND SANITIZER8 mL in 1 BOTTLE, SPRAYGEL810
75613-005-02HAND SANITIZER10 mL in 1 BOTTLE, SPRAYGEL1010
75613-005-03HAND SANITIZER30 mL in 1 BOTTLEGEL3010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75613-005HAND SANITIZER (ALCOHOL) GEL [NINGBO LANZI COSMETIC TECHNOLOGY CO., LTD]10Legacy NDC, 3 package rows20200623_8ea55574-404d-49e2-a8b0-80e9e366c77c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75613-00575613-005-01, 75613-005-02, 75613-005-03

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
f22c535f-0233-41ca-8647-49ae1703e0a78ea55574-404d-49e2-a8b0-80e9e366c77c2020-06-23WarningsExact identifier
spl id: f22c535f-0233-41ca-8647-49ae1703e0a7
spl set id: 8ea55574-404d-49e2-a8b0-80e9e366c77c

Reported adverse events (FAERS/openFDA)#

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