DISNEY FROZEN STRAWBERRY HAND SANITIZER- benzalkonium chloride gel

Disney Frozen Strawberry Hand Sanitizer by

Drug Labeling and Warnings

Disney Frozen Strawberry Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SHENZHEN LANTERN SCIENCE CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Antibacterial

To decrease bacteria on skin that could cause disease

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE.......0.1%

DOSAGE AND ADMINISTRATION

Rub a dime sized drop into hands

For children under 6 use unde adult supervision

WARNINGS

For external use only - hands

Keep out of eyes.

Avoid contact with broken skin.

Do not inhale or ingest

If swallowed get medical help or contact a poison control center right away

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

For children under 6, use under adult supervision

INDICATIONS AND USAGE

To decrease bacteria on skin that could cause disease.

INACTIVE INGREDIENTS

WATER (AQUA/EAU)
GLYCERIN
COCETH-7
PPG-1-PEG-9 LAURYL GLYCOL ETHER
CARBOMER
PEG-40 HYDROGENATED CASTOR OIL
FRAGRANCE (PARFUM)
SODIUM HYDROXIDE

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

DISNEY FROZEN STRAWBERRY HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
COCETH-7 (UNII: 58Y261JLH5)
CARBOMER 1342 (UNII: 809Y72KV36)
GLYCERIN (UNII: PDC6A3C0OX)
PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CASTOR OIL (UNII: D5340Y2I9G)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	red (RED 40) , red (RED 33) , blue (BLUE 1) , yellow (YELLOW 5)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-022-02	60 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/14/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/14/2016

Labeler - SHENZHEN LANTERN SCIENCE CO., LTD (421222423)

Establishment
Name	Address	ID/FEI	Business Operations
SHENZHEN LANTERN SCIENCE CO., LTD		421222423	manufacture(54860-022)