MARVELS ULTIMATE SPIDER MAN STRAWBERRY SCENTED HAND SANITIZER- 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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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

Spider man

MARVELS ULTIMATE SPIDER MAN STRAWBERRY SCENTED HAND SANITIZER 
benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
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
Colorred (RED 40) , red (RED 33) , blue (BLUE 1) , yellow (YELLOW 5) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54860-021-0160 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/14/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/14/2016
Labeler - SHENZHEN LANTERN SCIENCE CO., LTD (421222423)
Establishment
NameAddressID/FEIBusiness Operations
SHENZHEN LANTERN SCIENCE CO., LTD421222423manufacture(54860-021)

Revised: 3/2016
Document Id: 2e0769a3-6eb7-0eef-e054-00144ff88e88
Set id: 2e071d6e-e1de-05c9-e054-00144ff88e88
Version: 2
Effective Time: 20160314
 
SHENZHEN LANTERN SCIENCE CO., LTD