Disney Princess Antibacterial Hand Wipes

Manufacturer: Peachtree Playthings, Inc.
Effective date: 2020-12-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 22:48:10

Label at a glance#

ProductDisney Princess Antibacterial Hand Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Dosage and administration

adults and children 2 years and over Apply to hands Allow to dry without wiping children under 2 years ask a doctor before use

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

decreases bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any ingredients

When using this product

OTC - WHEN USING SECTION

do not get into your eyes. If contact occurs, rinse thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Use of the product by children should be supervised by an adult

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash develops and continues for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION


adults and children 2 years and over	Apply to hands Allow to dry without wiping
children under 2 years	ask a doctor before use

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Propylene Glycol, GLycerin, Ethylhexylglycerin, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate.

Package Labeling:20 wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3

Package Labeling:80 wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4

Products#

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

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

Disney Princess Antibacterial Hand Wipes
BENZALKONIUM CHLORIDE
WATER
PHENOXYETHANOL
PROPYLENE GLYCOL
GLYCERIN
ETHYLHEXYLGLYCERIN
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
44119-010	44119-010-01, 44119-010-02

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
WATER	059QF0KO0R	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
075a4e3f-d9db-5081-e063-6394a90a9ef2			b695be7d-c7e7-4484-e053-2995a90aea92	2023-10-10	Warnings	Exact identifier spl set id: b695be7d-c7e7-4484-e053-2995a90aea92

Reported adverse events (FAERS/openFDA)#

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