MY LITTLE PONY HAND SANITIZER 6 PACK- benzalkonium chloride gel

My little Pony Hand Sanitizer by

Drug Labeling and Warnings

My little Pony 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]

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose: Antibacterial

PURPOSE

Use

To decrease bacteria on the skin that could cause disease.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNINGS

Warnings

• for external use only-hands.
• keep out of eyes. avoid contact with broken skin.
• stop use and ask a Doctor if irritation or redness develops.
• do not inhale or ingest. if swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION

Directions

• Rub a dime sized drop into hands.
• For children under 6 use under adult supervision.

INACTIVE INGREDIENT

Inactive Ingredients

water (aqua/eau), glycerin, coceth-7, PPG-1-PEG-9 lauryl glycol ether, carbomer, hydrogenated castor oil, fragrance (parfum).

May Contain

Red 40 (CI 16035), Red 33 (CI 17200), Blue 1 (CI 42090), Yellow 5 (CI 19140).

INDICATIONS & USAGE

Hand Sanitizer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MY LITTLE PONY HAND SANITIZER  6 PACK
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-084
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 g  in 22 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYL FRAGMENT (UNII: 0KIZ9B76US)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor	BLUEBERRY, STRAWBERRY, BERRY, GRAPE, BUBBLE GUM, WATERMELON	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-084-01	22 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/10/2017

Labeler - Shenzhen Lantern Science Co., Ltd. (421222423)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co., Ltd.		421222423	manufacture(54860-084)