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ANTIBACTERIAL MANDARIN AND GRAPEFRUIT

Dosage form: liquid
Ingredients: TRICLOSAN 0.15mL in 100mL
Labeler: KMART CORPORATION
NDC Code: 49738-215

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 PRODUCTAVOID CONTACT WITH EYES.  IF CONTACT OCCURS, RINSE THROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION AND REDNESS DEVELOP.

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 THOROUGHLY.

QUESTIONS OR COMMENTS

1-800-842-7886

INACTIVE INGREDIENTS

Water (Aqua), Sodium Laureth Sulfate, Decyl Glucoside, Cocamidopropyl Betaine, Sodium Chloride, Cocamide MEA, Fragrance (Parfum), PEG-120 Methyl Glucose Dioleate, PEG- 18 Glyceryl Oleate/Cocoate, Aloe Barbadensis Leaf Juice, Polyquaternium-7, DMDM Hydantoin, Tetrasodium EDTA, Citric Acid, Red 33 (CI 17200), Yellow 6 (CI 15985).

ANTIBACTERIAL  MANDARIN AND GRAPEFRUIT
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49738-215
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 
DECYL GLUCOSIDE 
COCAMIDOPROPYL BETAINE 
SODIUM CHLORIDE 
COCO MONOETHANOLAMIDE 
PEG-120 METHYL GLUCOSE DIOLEATE 
1-GLYCERYL MONOOLEATE 
ALOE VERA LEAF 
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) 
DMDM HYDANTOIN 
EDETATE SODIUM 
CITRIC ACID MONOHYDRATE 
D&C RED NO. 33 
FD&C YELLOW NO. 6 
Packaging
#Item CodePackage Description
1NDC:49738-215-08221 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/07/2011
Labeler - KMART CORPORATION (008965873)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIOperations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

Revised: 07/2011
Document Id: 365013d1-6f01-4d6b-aabb-80ae1e0c63d5
Set id: 0eb81e92-198c-477a-857d-2607379a5330
Version: 1
Effective Time: 20110707
 
KMART CORPORATION

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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