GOJO Ultra Mild Antimicrobial Lotion Soap with Chloroxylenol

Manufacturer: GOJO Industries, Inc.
Effective date: 2026-03-05
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:48:59

Label at a glance#

ProductGOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol

Active ingredientCHLOROXYLENOL

Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

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 a small amount of product and work into a lather

• Rinse well and dry hands completely

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Coconut Acid, Oleic Acid, Sodium Sulfate, Ethanolamine, Cocamide MEA, Coco-Betaine, Propylene Glycol, Retinyl Palmitate, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Fragrance (Parfum)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
424daadb-95de-8ece-97f5-235e3f7f0001	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
21749-211-10	GOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol	1000 mL in 1 BAG	LIQUID	1000	3
21749-211-20	GOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol	2000 mL in 1 BAG	LIQUID	2000	3
21749-211-80	GOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol	800 mL in 1 BAG	LIQUID	800	3

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

GOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol
Chloroxylenol
WATER
COCONUT ACID
OLEIC ACID
SODIUM SULFATE
MONOETHANOLAMINE
COCO MONOETHANOLAMIDE
COCO-BETAINE
PROPYLENE GLYCOL
VITAMIN A PALMITATE
EDETATE SODIUM
.ALPHA.-TOCOPHEROL ACETATE
CORN OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
21749-211	21749-211-80, 21749-211-10, 21749-211-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCONUT ACID	40U37V505D	IACT
OLEIC ACID	2UMI9U37CP	IACT
SODIUM SULFATE	0YPR65R21J	IACT
MONOETHANOLAMINE	5KV86114PT	IACT
COCO MONOETHANOLAMIDE	C80684146D	IACT
COCO-BETAINE	03DH2IZ3FY	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
VITAMIN A PALMITATE	1D1K0N0VVC	IACT
EDETATE SODIUM	MP1J8420LU	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
CORN OIL	8470G57WFM	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB

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
GOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol	CHLOROXYLENOL	GOJO Industries, Inc.	150f808d-11c9-41d1-847e-0b7027515c19	2026-03-05	Warnings	Exact identifier ndc (package): 21749-211-10 ndc (package): 21749-211-20 ndc (package): 21749-211-80 ndc (product): 21749-211 ndc11 (package): 21749021110 ndc11 (package): 21749021120 ndc11 (package): 21749021180 spl id: 4c4890b6-96f8-0848-e063-6394a90a125b spl set id: 150f808d-11c9-41d1-847e-0b7027515c19

Reported adverse events (FAERS/openFDA)#

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