GOJO PCMX E-2 SANITIZING LTN SP- chloroxylenol liquid

GOJO PCMX E-2 Sanitizing Ltn Sp by

Drug Labeling and Warnings

GOJO PCMX E-2 Sanitizing Ltn Sp by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Chloroxylenol 0.3%

Purpose

Antimicrobial

Uses

• Handwash to help decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands
• Apply a small amount of product and work into a lather
• Rinse well and dry hands completely

Inactive ingredients

Water (Aqua), Coconut Acid, Oleic Acid, Sodium Sulfate, Ethanolamine, Cocamide MEA, Coco-Betaine, Propylene Glycol, Tetrasodium EDTA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOJO PCMX E-2 SANITIZING LTN SP 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-457
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.003 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCONUT ACID (UNII: 40U37V505D)
OLEIC ACID (UNII: 2UMI9U37CP)
SODIUM SULFATE (UNII: 0YPR65R21J)
MONOETHANOLAMINE (UNII: 5KV86114PT)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
Coco-Betaine (UNII: 03DH2IZ3FY)
Propylene Glycol (UNII: 6DC9Q167V3)
EDETATE SODIUM (UNII: MP1J8420LU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-457-80	800 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/25/2019
2	NDC: 21749-457-20	2000 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/25/2019
3	NDC: 21749-457-50	5000 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/25/2019
4	NDC: 21749-457-37	3780 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/25/2019
5	NDC: 21749-457-55	208000 mL in 1 PACKAGE; Type 0: Not a Combination Product	02/25/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/25/2019

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	MANUFACTURE(21749-457)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	label(21749-457) , pack(21749-457)