FDA.reportPublic FDA data

Antibacterial HAND SANITIZER

Manufacturer
Ningbo Lanzi Cosmetic Technology Co., Ltd
Effective date
2020-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:15

Label at a glance#

ProductAntibacterial HAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6 age use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing

Warnings

WARNINGS SECTION

For external use only - hands

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.

Do not inhale or ingest.

Stop use and ask a doctor if

skin irritation develops.

Other Information:

  • Do not store above 105℉
  • May discolor some fabrics.

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 allow to dry without wiping.
  • For children under 6 age use only under adult supervision.
  • Not recommended for infants.

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 GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75613-003-012022-01-28C16284748780-1d6a99b39-daff-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75613-003-01Antibacterial HAND SANITIZER54 mL in 1 BOTTLEGEL541

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75613-003ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [NINGBO LANZI COSMETIC TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20200606_612bf32d-1504-43a8-9d3a-a626cc33dbf5.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
75613-00375613-003-01

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
50d79fa5-5081-4de8-8ac8-03c8f79dc8b7612bf32d-1504-43a8-9d3a-a626cc33dbf52020-06-05WarningsExact identifier
spl id: 50d79fa5-5081-4de8-8ac8-03c8f79dc8b7
spl set id: 612bf32d-1504-43a8-9d3a-a626cc33dbf5

Reported adverse events (FAERS/openFDA)#

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