Hand Sanitizer

Manufacturer: DISNEY DESTINATIONS,LLC
Effective date: 2018-11-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:57:23

Label at a glance#

ProductHand Sanitizer

Active ingredientBENZETHONIUM CHLORIDE

Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:
Benzethonium Chloride 0.095%

OTC - PURPOSE SECTION

Purpose

Antiseptic

OTC - STOP USE SECTION

Stop using this product and consult a doctor 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.

DOSAGE & ADMINISTRATION SECTION

Directions

Rub dime sized amount between hands until dry.
For use by children under 6 years, adult supervision is required.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Fragrance, Glycerin, Methylisothiazolinone, PEG-40 Hydrogenated Castor Oil, Polyquatemium-37, Propylene Glycol, Triethanolamine, Water,

INDICATIONS & USAGE SECTION

Uses

To help reduce bacteria on hands.

WARNINGS SECTION

Warnings:

For external use only.

OTC - WHEN USING SECTION

When using this product,

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2104345	benzethonium chloride 0.095 % Topical Gel	PSN	1
2104345	benzethonium chloride 0.00095 MG/MG Topical Gel	SCD	1
2104345	benzethonium chloride 0.095 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72707-001-01	2020-01-31	C162847	48780-1	9d75b9d0-d432-f424-e053-dadaa90a57ce	7ba62c4e-b399-a614-e053-2a91aa0a1d64

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72707-001-01	Hand Sanitizer	29 mL in 1 BOTTLE, PLASTIC	GEL	29		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72707-001	HAND SANITIZER (BENZETHONIUM CHLORIDE) GEL [DISNEY DESTINATIONS,LLC]	1	Legacy NDC, 1 package rows	20181127_7ba62c4e-b399-a614-e053-2a91aa0a1d64.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Hand Sanitizer
BENZETHONIUM CHLORIDE
PROPYLENE GLYCOL
GLYCERIN
METHYLISOTHIAZOLINONE
POLYQUATERNIUM 37 (200 MPA.S)
BENZETHONIUM
WATER
TROLAMINE
POLYOXYL 40 HYDROGENATED CASTOR OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72707-001	72707-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
POLYQUATERNIUM 37 (200 MPA.S)	67C1D6YV24	IACT
BENZETHONIUM CHLORIDE	PH41D05744	ACTIB
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
7ba62c4e-b39a-a614-e053-2a91aa0a1d64			7ba62c4e-b399-a614-e053-2a91aa0a1d64	2018-11-27	Warnings	Exact identifier spl id: 7ba62c4e-b39a-a614-e053-2a91aa0a1d64 spl set id: 7ba62c4e-b399-a614-e053-2a91aa0a1d64

Reported adverse events (FAERS/openFDA)#

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