Maxim FDF

Manufacturer: Midlab Incorporated
Effective date: 2025-07-28
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 01:09:30

Label at a glance#

ProductMaxim FDF

Active ingredientCHLOROXYLENOL

Label structure9 sections

Indications and uses

• Handwash to help decrease bacteria on the skin.

Dosage and administration

• Apply a small amount of product to wet hands, work into lather for 30 seconds, 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 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Handwash to help decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.
Do not use in the eyes. In case of contact, immediately flush eyes with water.

OTC - ASK DOCTOR 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

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly.
• Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua) (7732-18-5), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycerin (56-81-5), Cocamidopropyl Hydroxysultaine (68139-30-0), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium Polyitaconate (26099-89-8), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1941461	chloroxylenol 0.1 % Medicated Liquid Soap	PSN	9
1941461	chloroxylenol 1 MG/ML Medicated Liquid Soap	SCD	9
1941461	chloroxylenol 0.1 % Medicated Liquid Soap	SY	9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70542-201-41	Maxim FDF	3.78 L in 1 BOTTLE, PLASTIC	SOAP	3.78		9
70542-201-55	Maxim FDF	208 L in 1 DRUM	SOAP	208		9

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Maxim FDF
chloroxylenol
COCAMIDOPROPYL HYDROXYSULTAINE
PROPANEDIOL
BRONOPOL
SODIUM C14-16 OLEFIN SULFONATE
GLYCERIN
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED)
WATER
PROPYLENE GLYCOL
METHYLISOTHIAZOLINONE
METHYLCHLOROISOTHIAZOLINONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70542-201	70542-201-41, 70542-201-55

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
COCAMIDOPROPYL HYDROXYSULTAINE	62V75NI93W	IACT
PROPANEDIOL	5965N8W85T	IACT
BRONOPOL	6PU1E16C9W	IACT
SODIUM C14-16 OLEFIN SULFONATE	O9W3D3YF5U	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED)	G7SW5QN7TT	IACT
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	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
Maxim FDF	CHLOROXYLENOL	Midlab Incorporated	83d26ca6-b075-edab-e053-2991aa0add3f	2025-07-28	Warnings	Exact identifier ndc (package): 70542-201-41 ndc (package): 70542-201-55 ndc (product): 70542-201 ndc11 (package): 70542020141 ndc11 (package): 70542020155 spl id: 3b00d424-86a6-00f7-e063-6294a90a980c spl set id: 83d26ca6-b075-edab-e053-2991aa0add3f

Reported adverse events (FAERS/openFDA)#

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