FDA.reportPublic FDA data

Vanilla Hand Sanitizer

Manufacturer
Shenzhen Lantern Science Co., Ltd.
Effective date
2018-02-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:23

Label at a glance#

ProductVanilla Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.1%

OTC - PURPOSE SECTION

Antibacterial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Warnings

  • for external use only
  • if irritation occurs discontinue use
  • keep out of eyes
  • avoid contact with broken skin
  • do not inhale or ingest
  • stop use and ask if doctor if skin irritation develops
  • keep out of reach of children
  • if swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Rub a dime sized drop into hands.
  • For children under 6 use under adult supervision.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

water/aqua, hydroxyethylcellulose, phenoxyethanol, fragrance/parfum, disodium edta

INDICATIONS & USAGE SECTION

To decrease bacteria on hands

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSN1
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCD1
1049228benzalkonium chloride 0.1 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-089-012022-01-28C16284748780-1d6a99b39-341c-a426-e053-dadaa90af4c264914c6a-aea3-3c30-e053-2a91aa0a88b0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-089-01Vanilla Hand Sanitizer30 mL in 1 BOTTLEGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-089VANILLA HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [SHENZHEN LANTERN SCIENCE CO., LTD.]1Legacy NDC, 1 package rows20180207_64914c6a-aea3-3c30-e053-2a91aa0a88b0.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
54860-08954860-089-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYETHYL ETHYLCELLULOSEZDN57Z154KIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
EDETATE DISODIUM7FLD91C86KIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT

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
64914c6a-aea4-3c30-e053-2a91aa0a88b064914c6a-aea3-3c30-e053-2a91aa0a88b02018-02-06WarningsExact identifier
spl id: 64914c6a-aea4-3c30-e053-2a91aa0a88b0
spl set id: 64914c6a-aea3-3c30-e053-2a91aa0a88b0

Reported adverse events (FAERS/openFDA)#

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