FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Ningbo Lanzi Cosmetic Technology Co., Ltd
Effective date
2020-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:24

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure6 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72% v/v

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to Helps reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only: hands.

Flammable. Keep away from heat or flame.

Do not use 

On children under the age of 2 months. On any open wounds.

When using this product

Keep out of eyes, ears, and mouth. In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness occurs. These may be signs of serious reaction.

Other Information:

Store between 50-86℉ (15-30℃) 。

Avoid freezing and excessive heat above 104℉ (40℃).

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 a dime size amount into hand. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallwing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbmer, Fragrance, Glycerin, Propylene Glycol, Triethanolamine, Disodium ETDA, Tocopheryl Acetate, Deionized Water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2277550ethanol 72 % Topical GelPSN1
2277550ethanol 0.72 ML/ML Topical GelSCD1
2277550ethanol 72 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75613-010-012022-01-28C16284748780-1d6a99b39-97e4-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75613-010-01HAND SANITIZER1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75613-010HAND SANITIZER (ALCOHOL) GEL [NINGBO LANZI COSMETIC TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20201025_b87287c3-b318-47b0-8293-abe866954df6.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
75613-01075613-010-01

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
EDETATE DISODIUM7FLD91C86KIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
GLYCERINPDC6A3C0OXIACT

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
5fe732c0-3ecd-482c-9726-cb895124691ab87287c3-b318-47b0-8293-abe866954df62020-10-24WarningsExact identifier
spl id: 5fe732c0-3ecd-482c-9726-cb895124691a
spl set id: b87287c3-b318-47b0-8293-abe866954df6

Reported adverse events (FAERS/openFDA)#

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