My Little Pony Hand Sanitizer 6 Pack (Benzalkonium Chloride) Gel [Shenzhen Lantern Science Co., Ltd.] -

MY LITTLE PONY HAND SANITIZER 6 PACK (BENZALKONIUM CHLORIDE) GEL [SHENZHEN LANTERN SCIENCE CO., LTD.]
PDF | XML

NDC	54860-084-01
Set ID	53fc602b-0e59-4d9b-e054-00144ff8d46c
Category	HUMAN OTC DRUG LABEL
Packager	Shenzhen Lantern Science Co., Ltd.
Generic Name
Product Class
Product Number
Application Number	PART333E

View All Sections

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

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

Ingredient Name	Strength
Inactive Ingredients
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

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

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

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

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

View All Sections

Medic