WINNING HANDS FOAMING ANTIBACTERIAL- benzalkonium chloride soap 
Betco Corporation, 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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Winning Hands Foaming Antibacterial

Winning Hands Foaming Antibacterial

​Active Ingredient

​Benzalkonium Chloride 0.13%

Winning Hands Foaming Antibacterial

Uses

Winning Hands Foaming Antibacterial

Warnings

Winning Hands Foaming Antibacterial

Directions

Winning Hands Foaming Antibacterial

Inactive Ingredients

Water, Potassium Cocoate, Propylene Glycol, Glycerin, Tetrasodium EDTA, Fragrance, Bronopol, Sodium Citrate,
Magnesium Nitrate, Sodium Hydroxyacetate, Ethanol, Aloe Barbadensis Leaf Juice, Trisodium Nitriloacetate,
FD&C Yellow #5, Sodium Hydroxide, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone,
FD&C Red #40.

Winning Hands Foaming Antibacterial

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400 Van Camp Road Bowling Green, Ohio 43402
Made In U.S.A. All Rights Reserved.

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Winning Hands Foaming Antibacterial

Purpose

Antibacterial

Winning Hands Foaming Antibacterial

KEEP OUT OF REACH OF CHILDREN

Winning Hands Foaming Antibacterial

Winning Hands Foaming Antibacterial

75155-00

Foaming Skin Cleanser with Triclosan

NET CONTENTS: 55 gallons (U.S./E.U.) 208 L

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WINNING HANDS FOAMING ANTIBACTERIAL 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-754
Route of AdministrationTopical
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 1.0 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)  
BRONOPOL (UNII: 6PU1E16C9W)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
SODIUM GLYCOLATE (UNII: B75E535IMI)  
ALCOHOL (UNII: 3K9958V90M)  
ALOE (UNII: V5VD430YW9)  
TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65601-754-541000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/12/2012
2NDC:65601-754-55208000 mL in 1 DRUM; Type 0: Not a Combination Product11/12/2012
3NDC:65601-754-043780 mL in 1 JUG; Type 0: Not a Combination Product11/12/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/12/2012
Labeler - Betco Corporation, Ltd. (024492831)
Registrant - Betco corporation, Ltd. (024492831)
Establishment
NameAddressID/FEIBusiness Operations
Betco Corpo, Ltd.024492831manufacture(65601-754) , pack(65601-754) , label(65601-754)

Revised: 2/2019
Document Id: 23d7d61c-26cb-44ba-91a3-76d50efcce8e
Set id: 9d18b802-266d-4524-8937-f0e560014b63
Version: 1
Effective Time: 20190214
 
Betco Corporation, Ltd.