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ANTIBACTERIAL FOAMING by TOPCO ASSOCIATES LLC

Medically reviewed on Nov 2, 2017

Dosage form: liquid
Ingredients: TRICLOSAN 0.6mL in 100mL
Labeler: TOPCO ASSOCIATES LLC
NDC Code: 36800-076

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.

DRUG FACTS

ACTIVE INGREDIENT

TRICLOSAN 0.6 PERCENT

PURPOSE

ANTIBACTERIAL

USES

HELPS REDUCE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES.  IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION AND REDNESS DEVELOPS AND LASTS.

DIRECTIONS

PUMP ONTO DRY HANDS, WORK INTO A LATHER AND RINSE THOROUGHLY.

STORE AT ROOM TEMPERATURE.

INACTIVE INGREDIENTSWATER, SODIUM XYLENESULFONATE, SODIUM LAURETH SULFATE, DIPROPYLENE GLYCOL, COCAMIDOPROPYL BETAINE, POLYSORBATE 20, FRAGRANCE, DISODIUM PHOSPHATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, RED 33 (CI 17200), YELLOW 5 (CI 19140).

FRONT AND BACK LABELS

ANTIBACTERIAL FOAMING  
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-076
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.6 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM XYLENESULFONATE 
DIPROPYLENE GLYCOL 
SODIUM LAURETH SULFATE 
COCAMIDOPROPYL BETAINE 
SODIUM PHOSPHATE, DIBASIC, DIHYDRATE 
CITRIC ACID MONOHYDRATE 
D&C RED NO. 33 
FD&C YELLOW NO. 5 
WATER 
POLYSORBATE 20 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:36800-076-08222 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/02/2011
Labeler - TOPCO ASSOCIATES LLC (006935977)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

 
TOPCO ASSOCIATES LLC

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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