GOJO Premium Foam Antibacterial Handwash

Manufacturer: GOJO Industries, Inc.
Effective date: 2019-05-15
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 00:21:02

Label at a glance#

ProductGOJO Premium Foam Antibacterial Handwash

Active ingredientCHLOROXYLENOL

Label structure7 sections

Dosage and administration

Wet hands Apply product and thoroughly cover hands with lather Rinse well and dry hands completely

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.5%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands
Apply product and thoroughly cover hands with lather
Rinse well and dry hands completely

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

GOJO Premium Foam Antibacterial Handwash
CHLOROXYLENOL
WATER
ALCOHOL
SODIUM LAURETH SULFATE
DISODIUM COCOAMPHODIACETATE
GLYCERIN
ISOPROPYL ALCOHOL
LACTIC ACID
FD&C RED NO. 4
FD&C YELLOW NO. 6

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
21749-185	21749-185-53, 21749-185-89

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CHLOROXYLENOL	0F32U78V2Q	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
DISODIUM COCOAMPHODIACETATE	18L9G3U51M	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
LACTIC ACID	33X04XA5AT	IACT
FD&C RED NO. 4	X3W0AM1JLX	IACT
FD&C YELLOW NO. 6	H77VEI93A8	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
cb943ca8-817f-4ff0-ab80-0c9b4010c3cc			974e4e28-0694-40b7-b3f2-aeb7a7a5992e	2023-06-08	Warnings	Exact identifier spl set id: 974e4e28-0694-40b7-b3f2-aeb7a7a5992e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.