Anti-Bacterial HAND SANITIZER

Manufacturer
DISNEY DESTINATIONS,LLC
Effective date
2025-04-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:58:47

Label at a glance#

ProductAnti-Bacterial HAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

To help reduce bacteria on hands.

Dosage and administration

Place enough to cover both hands in the palm, and rub hands together until dry. Children under 6 years of age should be supervised by adults when applying this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 63%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on hands.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from fire, flame and direct sunlight.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes and lips.
  • If contact occurs, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children If swallowed, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough to cover both hands in the palm, and rub hands together until dry.
  • Children under 6 years of age should be supervised by adults when applying this product.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

aminomethyl propanol, carbomer, denatonium benzoate, glycerin, propylene glycol, water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1094724ethanol 63 % Topical GelPSN2
1094724ethanol 0.63 ML/ML Topical GelSCD2
1094724ethanol 63 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72707-029-012025-04-07C16284748780-12cef2736-752d-d83d-e063-dadaa90ab31f72707-029, Anti-Bacterial HAND SANITIZER
72707-029-012025-01-30C16284748780-12cef2736-752d-d83d-e063-dadaa90ab31f72707-029, Anti-Bacterial HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72707-029-01Anti-Bacterial HAND SANITIZER29 mL in 1 BOTTLE, PLASTICGEL292

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72707-029ANTI-BACTERIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [DISNEY DESTINATIONS,LLC]2Current NDC, Legacy NDC, 1 package rows20250409_ae739bda-edf3-634b-e053-2a95a90a7385.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
72707-02972707-029-01

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
Anti-Bacterial HAND SANITIZERETHYL ALCOHOLDISNEY DESTINATIONS,LLCae739bda-edf3-634b-e053-2a95a90a73852025-04-07WarningsExact identifier
ndc (package): 72707-029-01
ndc (product): 72707-029
ndc11 (package): 72707002901
spl id: 3239c530-a116-8e4e-e063-6294a90a95a1
spl set id: ae739bda-edf3-634b-e053-2a95a90a7385

Reported adverse events (FAERS/openFDA)#

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