ULTRAGREEN ANTIBACTERIAL- triclosan liquid

Ultragreen Antibacterial by

Drug Labeling and Warnings

Ultragreen Antibacterial by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Triclosan, 0.15

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

For hand washing to reduce bacteria on the skin

WARNINGS

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.

DOSAGE & ADMINISTRATION

Directions

Apply soap to dry hands

Add water

Lather for 30 seconds

Rinse and dry

INACTIVE INGREDIENT

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)

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

ULTRAGREEN ANTIBACTERIAL 
triclosan liquid

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

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

Labeler - Deb USA, Inc. (607378015)

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