Champion Ultra Clean Fragrance and Dye Free

Manufacturer: Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
Effective date: 2020-02-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:40:09

Label at a glance#

ProductChampion Ultra Clean Fragrance and Dye Free

Active ingredientCHLOROXYLENOL

Label structure9 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

-Apply to wet hands. -Work into a lather and rinse thoroughly. -Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol.......0.3%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When Using this Product

GENERAL PRECAUTIONS SECTION

Avoid contact with the eyes.

In case of eye contact, flush eyes with water.

Do not ingest.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help

or contact a Posion Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

-Apply to wet hands.

-Work into a lather and rinse thoroughly.

-Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Glycerine, Aloe Vera.

Champion Ultra Clean Fragrance and Dye Free

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Champion Ultra Clean Fragrance and Dye Freeimage description

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Champion Ultra Clean Fragrance and Dye Free
Chloroxylenol
Water
SODIUM LAURETH SULFATE
SODIUM CHLORIDE
COCAMIDOPROPYL BETAINE
GLYCERIN
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50241-018	50241-018-01, 50241-018-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CHLOROXYLENOL	0F32U78V2Q	ACTIB
Water	059QF0KO0R	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT

Source Document#

Source XML · Source PDF

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
aae60040-f9a8-49a2-e053-2a95a90ac397			0dec033a-c2e9-4e23-949e-b83e1e721450	2020-07-20	Warnings	Exact identifier spl set id: 0dec033a-c2e9-4e23-949e-b83e1e721450

Reported adverse events (FAERS/openFDA)#

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