BRIGHT SOLUTIONS ANTIBACTERIAL - triclosan liquid
Deb USA, 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.

----------

Drug Facts

Active ingredient

Triclosan, 0.30%

Purpose

Antibacterial

Uses

For hand washing to reduce bacteria on the skin

Warnings

For external use only

When using this product

Avoid contact with eyes. In case of eye contact, flush with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply foaming cleanser to dry hands

Rub hands together to spread lather

Wash for 15-20 seconds

Rinse and dry hands thoroughly

Inactive ingredients

Water, Sodium Laureth Sulfate, Propylene Glycol, PPG-24-Glycereth-24, Cocamidopropyl Betaine, Tetrasodium EDTA, 2-Bromo-2-nitropropane-1, 3-diol, Fragrance, Citric Acid, Green 5 (CI 61570), Yellow 5 (CI 19140).

Bright Solutions

Antibacterial Foam Soap

Ideal for use where antibacterial action is desired

A high-quality, foam soap that is 99.99% effective against common bacteria.

deb foam technology

Made in USA

Distributed by:

Kelsan Inc.

5109 National Drive

Knoxville, TN 37914

800-624-7237

59257

1 Liter

33.8 Fluid Ounces

Rev. 08-11

container label

BRIGHT SOLUTIONS ANTIBACTERIAL
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11084-052
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	0.30 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
EDETATE SODIUM (UNII: MP1J8420LU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11084-052-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/15/2011	10/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	08/15/2011	10/01/2016

Labeler - Deb USA, Inc. (607378015)

Name	Address	ID/FEI	Business Operations
Establishment
Deb USA, Inc.		078805627	manufacture(11084-052)

Revised: 10/2017

Document Id: 05871739-f29c-4135-9a85-f7b0324b3dd9

Set id: 19ef76e0-ce9a-4d53-910c-452d127d18a2

Version: 4

Effective Time: 20171011

Deb USA, Inc.