Disney Minnie mouce strawberry scented hand sanitizer

Manufacturer: Yuyao Jessie Commodity Co.,Ltd. | Townley Inc.
Effective date: 2018-11-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:45:11

Label at a glance#

ProductDisney Minnie mouce strawberry scented hand sanitizer 01

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Contacts and useful links#

PhoneLabel contact1-212-779-0544

Label contents#

Full prescribing information#

Active ingredient purpose

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1% Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For external use only-hands

keep out of eyes- avoid contact with broken skin

Stop use and ask a dosctor if irritation or radness develops

Do not inhale or ingest. If swallowed, get medical help or contact a poison control right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For children under 6 use under adult supervision

Inactive ingredients

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER, GLYCERIN, COCETH-7, PPG-1-PEG-9 LAURYL GLYCOL ETHER, CARBOMER, SODIUM HYDROXIDE, PEG-40 HYDROGENATED CASTOR OIL, FRAGRANCE (PARFUM).
MAY CONTAIN: RED 40, RED 33, BLUE 1, YELLOW 5.

Questions?

OTC - QUESTIONS SECTION

1-212-779-0544 weekdays

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

51414-108-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51414-108-01	2022-01-28	C162847	48780-1	d6a99b39-eb0e-a426-e053-dadaa90af4c2	7bda9dd7-42d1-a366-e053-2991aa0a817d

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Disney Minnie mouce strawberry scented hand sanitizer 01
Benzalkonium Chloride
COCETH-7
PPG-1-PEG-9 LAURYL GLYCOL ETHER
WATER O-18
GLYCERIN
CARBOMER 934
SODIUM HYDROXIDE
HYDROGENATED CASTOR OIL
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
MYRISTICA FRAGRANS FRUIT
FD&C RED NO. 40
D&C RED NO. 33
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51414-108	51414-108-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
COCETH-7	58Y261JLH5	IACT
PPG-1-PEG-9 LAURYL GLYCOL ETHER	5R8J43K25L	IACT
WATER O-18	7QV8F8BYNJ	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER 934	Z135WT9208	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
MYRISTICA FRAGRANS FRUIT	GOO22BTU71	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
D&C RED NO. 33	9DBA0SBB0L	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
7bda9dd7-42c7-a366-e053-2991aa0a817d			7bda9dd7-42d1-a366-e053-2991aa0a817d	2018-11-29	Warnings	Exact identifier spl id: 7bda9dd7-42c7-a366-e053-2991aa0a817d spl set id: 7bda9dd7-42d1-a366-e053-2991aa0a817d

Reported adverse events (FAERS/openFDA)#

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