FDA.reportPublic FDA data

Disney Princess Antibacterial Hand Wipes

Manufacturer
Zhejiang Youquan Care Products Technology Co., Ltd.
Effective date
2022-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:48:14

Label at a glance#

ProductDisney Princess Antibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 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

Warning

WARNINGS SECTION

For external use only
Do not use if you are allergic to any ingredients When using this product do not get into your eyes. lf contact occurs, rinse thoroughly with water.
Use of this product by children should be supervised by an adult.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this out of reach of children.f swallowed, get medical help
or contact a Poison Control Center immediately.

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 LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77465-00577465-005-02

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
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
d599ed43-7540-ee2b-e053-2a95a90a61abb9d9153e-8622-7cdb-e053-2a95a90aef9f2022-01-15WarningsExact identifier
spl id: d599ed43-7540-ee2b-e053-2a95a90a61ab
spl set id: b9d9153e-8622-7cdb-e053-2a95a90aef9f

Reported adverse events (FAERS/openFDA)#

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