Active ingredient

Chloroxylenol 0.5%

Purpose

Antimicrobial

Use

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

Warnings

For external use only

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

Stop use and ask a doctor ifirritation 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 product and thoroughly cover hands with lather.
Rinse well and dry hands completely.

Inactive ingredients

Water (Aqua), Alcohol, Lauric Acid, Ethanolamine, Dipropylene Glycol, Lactic Acid, Poloxamer 124, Isopropyl Alcohol, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Fragrance (Parfum), Methylparaben, Propylparaben, Green 3 (CI 42053), Red 33 (CI 17200)

Product Label

GOJO ANTIMICROBIAL FOAM HANDWASH WITH PCMX
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:21749-521
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.005 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
LAURIC ACID (UNII: 1160N9NU9U)
MONOETHANOLAMINE (UNII: 5KV86114PT)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
LACTIC ACID (UNII: 33X04XA5AT)
POLOXAMER 124 (UNII: 1S66E28KXA)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
SODIUM SULFITE (UNII: VTK01UQK3G)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM SULFATE (UNII: 0YPR65R21J)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:21749-521-53	535 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2014	12/02/2024
2	NDC:21749-521-97	700 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2014	07/31/2021
3	NDC:21749-521-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2014	06/30/2023
4	NDC:21749-521-90	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	07/30/2014

Labeler - GOJO Industries, Inc. (004162038)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		036424534	manufacture(21749-521)

Name	Address	ID/FEI	Business Operations
Establishment
GOJO Industries, Inc.		088312414	label(21749-521) , pack(21749-521)

GOJO Antimicrobial Foam Handwash with PCMX

Active ingredient

Purpose

Use

Warnings

Directions

Inactive ingredients