ANTIBACTERIAL HAND SP WITH LIGHT MOISTURIZERS  - triclosan liquid 
SAM'S WEST INC.

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.

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DRUG FACTS

ACTIVE INGREDIENT

TRICLOSAN 0.115 PERCENT

PURPOSE

ANTIBACTERIAL

USES

FOR HANDWASHING TO DECREASE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

DO NOT GET INTO EYES.  IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

KEEP OUT OF REACH OF CHILDREN.

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS.

DIRECTIONS:

INACTIVE INGREDIENTS

WATER, SODIUM LAURETH SULFATE, LAURAMIDE DEA, COCAMIDOPROPYL BETAINE, HYDROLYZED VEGETABLE PROTEIN, SACCHAROMYCES,   POLYQUATERNIUM-7,  CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT, SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, GLYCERIN, TOCOPHERYL ACETATE, RETINYL PALMITATE, ASCORBYL PALMITATE, NIACINAMIDE, TETRASODIUM EDTA, SODIUM CHLORIDE, DMDM HYDANTOIN, CITRIC ACID, FRAGRANCE, YELLOW 5 (CI 19140), RED 40 (CI 16035),  RED 33 (CI 17200).

IMAGE OF MEMBER'S MARK ANTIBACTERIAL HAND SP WITH LIGHT MOISTURIZERS

ANTIBACTERIAL HAND SP WITH LIGHT MOISTURIZERS  
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68196-140
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.115 L  in 100 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SOY PROTEIN (UNII: R44IWB3RN5)  
SACCHAROMYCES LYSATE (UNII: R85W246Z1C)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
NIACINAMIDE (UNII: 25X51I8RD4)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68196-140-802.36 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/18/2011
Labeler - SAM'S WEST INC. (051957769)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture

Revised: 1/2011
Document Id: 243b4126-e3dd-4056-ba8a-1ed691248ee6
Set id: 8e1cd1ff-3e99-4679-9b24-1b04887a2bd2
Version: 1
Effective Time: 20110118
 
SAM'S WEST INC.