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ANTIBACTERIAL by AMERICAN SALES COMPANY

Medically reviewed on June 22, 2017

Dosage form: liquid
Ingredients: TRICLOSAN 0.15mL in 100mL
Labeler: AMERICAN SALES COMPANY
NDC Code: 41520-282

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 0.15%

PURPOSE

ANTIBACTERIAL

USES

FOR WASHING TO DECREASE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

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

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

PUMP ONTO WET HANDS, WORK INTO A LATHER, RINSE THROUGHLY.

WATER, SODIUM LAURETH SULFATE, SODIUM COCOYL SARCOSINATE, COCAMIDOPROPYL BETAINE, FRAGRANCE, PYRUS MALUS (APPLE) FRUIT EXTRACT, SODIUM PCA, BETAINE, SORBITOL, GLYCINE, ALANINE, PROLINE, SERINE, THREONINE, ARGININE, LYSINE, GLUTAMIC ACID, ALOE BARBADENSIS LEAF JUICE, PEG-120 METHYL GLUCOSE DIOLEATE, PEG-7 GLYCERYL COCOATE, TETRASODIUM EDTA, CITRIC ACID, SODIUM CHLORIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.

ANTIBACTERIAL 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-282
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.15 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
COCAMIDOPROPYL BETAINE 
APPLE 
SODIUM PYRROLIDONE CARBOXYLATE 
BETAINE 
SORBITOL 
GLYCINE 
ALANINE 
PROLINE 
SERINE 
THREONINE 
ARGININE 
LYSINE 
GLUTAMIC ACID 
ALOE VERA LEAF 
PEG-120 METHYL GLUCOSE DIOLEATE 
PEG-7 GLYCERYL COCOATE 
EDETATE SODIUM 
CITRIC ACID MONOHYDRATE 
SODIUM CHLORIDE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:41520-282-08236 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/22/2011
Labeler - AMERICAN SALES COMPANY (809183973)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

 
AMERICAN SALES COMPANY

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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