ULTRAGREEN 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.

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Drug Facts

Active ingredient

Triclosan, 0.15

Purpose

Antibacterial

Uses

For hand washing to reduce bacteria on the skin

Warnings

For external use only

When using this product

Avoid contact with the 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 soap to dry hands

Add water

Lather for 30 seconds

Rinse and dry

Inactive ingredients

Water, Sodium Laureth Sulfate, Cocamide DEA, Propylene Glycol, Sodium Chloride, Chloroxylenol, Acrylic Copolymer, Tetrasodium EDTA, Citric Acid, Fragrance, Sodium Hydroxide, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, Green 5 (CI 61570), Yellow 5 (CI 19140)

deb

UltraGreen

Antibacterial Hand Soap

99.9% Effective against many disease causing germs and bacteria

Pleasant fragrance

Clean rinsing

Ideal for all types of end users including Commercial Office Buildings, Public Facilities and anywhere refillable dispensing systems are installed

1 Gallon

1.78 Liters

75105

Made in USA

Deb USA, Inc.

Charlotte, NC 28217

1-800-248-7190

www.debgroup.com

Rev. 06-12

75105-ULTRAGREEN Pour 1gal-V7.jpg

ULTRAGREEN ANTIBACTERIAL
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11084-575
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	.15 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
Sodium Laureth Sulfate (UNII: BPV390UAP0)
Coco Diethanolamide (UNII: 92005F972D)
Propylene Glycol (UNII: 6DC9Q167V3)
Sodium Chloride (UNII: 451W47IQ8X)
Chloroxylenol (UNII: 0F32U78V2Q)
Edetate Sodium (UNII: MP1J8420LU)
Anhydrous Citric Acid (UNII: XF417D3PSL)
Sodium Hydroxide (UNII: 55X04QC32I)
D&C Green No. 5 (UNII: 8J6RDU8L9X)
FD&C Yellow No. 5 (UNII: I753WB2F1M)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
Magnesium Nitrate (UNII: 77CBG3UN78)
Magnesium Chloride (UNII: 02F3473H9O)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11084-575-05	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/20/2012	08/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/20/2012	08/01/2020

Labeler - Deb USA, Inc. (607378015)

Name	Address	ID/FEI	Business Operations
Establishment
Deb USA, Inc.		078805627	manufacture(11084-575)

Revised: 10/2017

Document Id: 17df196c-cd26-4533-83f9-f9e7c55cea03

Set id: a7aed80c-2cca-4798-b3c5-acfa302c3a86

Version: 15

Effective Time: 20171026

Deb USA, Inc.