BERRY SCENTED HAND SANITIZER GIRL- benzalkonium chloride gel
Shenzhen Lantern Science Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Use

To decrease bacteria on the skin that could cause disease.

keep out of reach of children

May Contain

Red 40 (Cl 16035)

Red 33 (Cl 17200)

Blue 1 (Cl42045)

Yellow 5 (Cl 19140)

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.

Directions

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

Inactive Ingredients

water (aqua/eau), glycerin, coceth-7, ppg-1-peg-9 lauryl glycol etyher, carbomer, sodium hydroxide, peg-40 hydrogenated castor oil, fragrance/parfum.

label image

BERRY SCENTED HAND SANITIZER GIRL
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54860-018
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.06 mg in 59 mg

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
COCETH-7 CARBOXYLIC ACID (UNII: 35KO064932)
PPG-1 TRIDECETH-6 (UNII: 1K7417JX6Q)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
FD&C RED NO. 40 (UNII: WZB9127XOA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color		Score
Shape		Size
Flavor	STRAWBERRY, BERRY, APPLE, RASPBERRY	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54860-018-01	59 mg in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	05/29/2013

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

Name	Address	ID/FEI	Business Operations
Establishment
Shenzhen Lantern Science Co., Ltd.		421222423	manufacture(54860-018)