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ANTIBACTERIAL REFILL by KMART CORPORATION

Dosage form: liquid
Ingredients: TRICLOSAN 0.15L in 100L
Labeler: KMART CORPORATION
NDC Code: 49738-216

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 HAND WASHING TO DECREASE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

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

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION AND REDNESS DEVELOPS.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

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

QUESTIONS OR COMMENTS

1-866-842-7886

INACTIVE INGREDIENTS

WATER, SODIUM C14-16 OLEFIN SULFONATE, LAURAMIDE DEA, SODIUM CHLORIDE, COCAMIDOPROPYL BETAINE, FRAGRANCE, CITRIC ACID, DMDM HYDANTOIN, GLYCERIN, TETRASODIUM EDTA, POLYQUATERNIUM-7, SILK PEPTIDE, HYDROLYZED SILK PROTEIN, ALOE BARBADENSIS LEAF JUICE, RED 40 (CI 16035), YELLOW 5 (19140), RED 33 (CI 17200)

ANTIBACTERIAL   REFILL
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49738-216
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.15 L  in 100 L
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM C14 OLEFIN SULFONATE 
LAURIC DIETHANOLAMIDE 
SODIUM CHLORIDE 
COCAMIDOPROPYL BETAINE 
CITRIC ACID MONOHYDRATE 
DMDM HYDANTOIN 
GLYCERIN 
EDETATE SODIUM 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) 
BOMBYX MORI FIBER 
BOMBYX MORI FIBER 
ALOE VERA LEAF 
FD&C YELLOW NO. 5 
D&C RED NO. 33 
FD&C RED NO. 40 
Packaging
#Item CodePackage Description
1NDC:49738-216-080.221 L in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/02/2011
Labeler - KMART CORPORATION (008965873)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

Revised: 06/2011
 
KMART CORPORATION

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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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