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ANTIBACTERIAL FOAMING OLIVE AND ALOE

Medically reviewed on January 22, 2018

Dosage form: liquid
Ingredients: TRICLOSAN 0.3mL in 100mL
Labeler: AMERICAN SALES COMPANY
NDC Code: 41520-170

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 0.3 PERCENT

PURPOSE

ANTISEPTIC

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 THOROUGHLY.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE.

INACTIVE INGREDIENTSWATER, SODIUM LAURETH SULFATE, GLYCERETH-26, DISODIUM LAURETH SULFOSUCCINATE, COCAMIDOPROPYL BETAINE, FRAGRANCE, PROPYLENE GLYCOL, PANTHENOL, ALOE BARBADENSIS LEAF JUICE, XANTHAN GUM, BENZOPHENONE-4, IMIDAZOLIDYNL UREA, DMDM HYDANTOI N, PEG-120 METHYL GLUCOSE DIOLEATE, PEG-7 GLYCERYL COCOATE, POLYSORBATE 20, TETRASODIUM EDTA, CITRIC ACID, BLUE 1 (CI 42090), YELLOW 10 (CI 47005).

ANTIBACTERIAL FOAMING   OLIVE AND ALOE
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41520-170
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.3 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
GLYCERETH-26 
DISODIUM LAURETH SULFOSUCCINATE 
COCAMIDOPROPYL BETAINE 
PROPYLENE GLYCOL 
PANTHENOL 
ALOE VERA LEAF 
XANTHAN GUM 
SULISOBENZONE 
IMIDUREA 
DMDM HYDANTOIN 
PEG-120 METHYL GLUCOSE DIOLEATE 
GLYCERYL COCOATE 
POLYSORBATE 20 
EDETATE SODIUM 
ANHYDROUS CITRIC ACID 
FD&C BLUE NO. 1 
D&C YELLOW NO. 10 
Packaging
#Item CodePackage Description
1NDC:41520-170-08236 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/21/2011
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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Further information

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

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