Drug Labeling and Warnings

Drug Details

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ANTIBACTERIAL BODY WASH- benzalkonium chloride lotion 
Topco Associates LLC

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 0.13%

Purpose

Antibacterial

Use

to decrease bacteria on the skin

Warnings

For external use only

When using this product

  • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • work a small amount into a lather
  • scrub thoroughly
  • rinse

inactive ingredients

water, PEG-120 methyl glucose dioleate, cetrimonium chloride, glycerin, lauramidopropylamine oxide, cocamide MEA, fragrance, sodium sulfate, myristamidopropylamine oxide, sodioum chloride, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

Questions?

1-888-423-0139

TopCare

Experience a whole new feeling of invigorating freshness with Antibacterial Body Wash. Enjoy the tantalizing fragrance of our moisturizing, antibacterial formula that will caress your skin and leave it satiny soft and clean.

DISTRIBUTED BY TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE, IL 60007

1-888-423-0139  TOPCO

[email protected]

principal display panel

TopCare

ANTIBACTERIAL BODY WASH

antibacterial cleanser plus moisturizer

SPRING FRESH

21 FL OZ (1 PT 5 FL OZ) 621 mL

image description

ANTIBACTERIAL BODY WASH 
benzalkonium chloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 36800-942
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.313 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 36800-942-56621 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/14/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/14/2014
Labeler - Topco Associates LLC (006935977)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon088520668manufacture(36800-942)

Revised: 12/2018
 
Topco Associates LLC


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