ANTIBACTERIAL  WITH LIGHT MOISTURIZERS- triclosan soap 
BJWC

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 Box - Back Label

Active Ingredient

Triclosan 0.115%

Purpose

- Antibacterial.



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 ingestions, get medical help or contact a Poison Control Center immediately.

Questions/Comments?

1-800-934-1204

Directions

Apply to wet hands, lather and rinse thoroughly.

Uses

To help reduce bacteria on the skin

Inactive Ingredeints

Water (Aqua), Sodium Laureth Sulfate, Lauramide DEA, Cocamidopropyl Betaine, Decyl Glucoside, Polyquaternium-7, Saccharomyces, Hydrolyzed Vegetable Protein, Camellia Sinensis (Green Tea) Leaf Extract, Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Retinyl Palmitate, Ascorbyl Palmitate, Niacinamide, Tetrasodium EDTA, Sodium Chloride, Fragrance (Parfum), DMDM Hydantoin, Citric Acid, Red 33 (CI 17200), Blue 1 (CI 42090).

Package Front and Back Labels

bj1g.jpg1Gal Front and Back Labels

ANTIBACTERIAL   WITH LIGHT MOISTURIZERS
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68391-141
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.115 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
NIACINAMIDE (UNII: 25X51I8RD4)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68391-141-503780 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/23/2010
Labeler - BJWC (159082692)

Revised: 7/2010
Document Id: 46451256-08fe-4e9e-a0c9-f486368c62c5
Set id: c0564387-7695-411f-97f6-f84712647770
Version: 1
Effective Time: 20100723
 
BJWC