ANTIBACTERIAL MOISTURIZING ALOE AND VITAMIN E- benzalkonium chloride liquid 
Brands International Corporation

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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Germs be Gone Antibacterial Hand Soap

Benzalkonium Chloride - 0.13%

Purpose - Antiseptic Skin cleanser

Effective in destroying (harmful) bacteria to provide antiseptic cleansing

Warnings For external use only

Stop use and ask a doctor if irritation or redness develops

When using this product

Keep out of reach of children If swallowed get medical help or contact a Poison Control Center right away

Directions

Lauramidopropylamine oxide, Lauryl Glucoside, PEG-150 distearate, Glycol Stearate, Perfume, PEG-7 glycerly cocoate, Cetrimonium Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Isopropyl myristate, Tocopheryl Acetate.

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ANTIBACTERIAL MOISTURIZING  ALOE AND VITAMIN E
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50157-509
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
GLYCOL STEARATE (UNII: 0324G66D0E)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50157-509-373780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2020
2NDC:50157-509-23236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2020
3NDC:50157-509-44443 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2020
4NDC:50157-509-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/17/2020
Labeler - Brands International Corporation (243748238)

Revised: 9/2020
Document Id: af873fa4-b5c0-1872-e053-2995a90a70e0
Set id: af87156e-a460-9f09-e053-2a95a90adb3d
Version: 1
Effective Time: 20200917
 
Brands International Corporation