DYNAREX GREEN- chloroxylenol liquid

Dynarex Green by

Drug Labeling and Warnings

Dynarex Green by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                         Purpose

Chloroxylenol 0.15%                   Antiseptic

WARNINGS

• For external use only
• When using this product avoid contact with eyes. In case of contact, flush with water.

PURPOSE

An antiseptic handwash.

Stop use and ask a doctor if

Stop use and ask a doctor if irritation and redness develop.

INDICATIONS & USAGE

Cleaning and antiseptic cleansing of hands and skin.

DOSAGE & ADMINISTRATION

• Wet hands and forearms. Apply 5 milliliters (teaspoon) or palmful to hands and forearms. Scrub thoroughly for 1 minute. Rinse and repeat.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN, if swallowed get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENTS

Inactive ingredients: Citric acid, Cocamidopropyl betaine, Cocmide DEA, D&C Red #33, Disodium EDTA, Frgarance, Glycerin, Sodium chloride, Sodium Lauryl Sulphate, Sodium o-phenylphenate, water.

PRINCIPAL DISPLAY PANEL

Dynarex Antibacterial Soap

1438 Soap.jpg

INGREDIENTS AND APPEARANCE

DYNAREX GREEN 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-318
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)
SODIUM O-PHENYLPHENATE (UNII: KFV9K7N7UI)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-318-01	221 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/13/2017

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)