GOJO PREMIUM FOAM ANTIBACTERIAL HANDWASH- chloroxylenol liquid

GOJO Premium Foam Antibacterial Handwash by

Drug Labeling and Warnings

GOJO Premium Foam Antibacterial Handwash 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 0.5%

Purpose

Antimicrobial

Use

• 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 product and thoroughly cover hands with lather
• Rinse well and dry hands completely

Inactive ingredients

Water (Aqua), Alcohol, Sodium Laureth Sulfate, Disodium Cocoamphodiacetate, Glycerin, Isopropyl Alcohol, Lactic Acid, Fragrance (Parfum), Red 4 (CI 14700), Yellow 6 (CI 15985)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOJO PREMIUM FOAM ANTIBACTERIAL HANDWASH 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-185
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	.05 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LACTIC ACID (UNII: 33X04XA5AT)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-185-53	222 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2019
2	NDC: 21749-185-89	1200 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/15/2019

Labeler - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-185)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		088312414	label(21749-185) , pack(21749-185)