MedPath

Chloroxylenol

Generic Name
Chloroxylenol
Brand Names
Cortane-B
Drug Type
Small Molecule
Chemical Formula
C8H9ClO
CAS Number
88-04-0
Unique Ingredient Identifier
0F32U78V2Q

Overview

Chloroxylenol, or para-chloro-meta-xylenol (PCMX), is an antiseptic and disinfectant agent used for skin disinfection and surgical instruments. It is found in antibacterial soaps, wound-cleansing applications, and household antiseptics. The halophenol is shown to be most effective against Gram positive bacteria where it disrupts the cell wall due to its phenolic nature . Chloroxylenol is on the World Health Organization's List of Essential Medicines.

Indication

The predominant medical applications for which chloroxylenol is formally indicated for therapeutic use is as an application to the skin for use in cuts, bites, stings, abrasions, and for use as antiseptic hand cleaner .

Associated Conditions

  • Skin Infections

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
First Medical Infection Control Associates, Inc.
68663-876
TOPICAL
3 mg in 1 mL
4/22/2025
Pro Chem, Inc.
63830-544
TOPICAL
3 mg in 1 mL
4/22/2025
ABC Compounding Co., Inc.
62257-161
TOPICAL
3 mg in 1 mL
4/22/2025
Costco Wholesale Corporation
63981-933
TOPICAL
3 mg in 1 mL
3/31/2025
The Procter & Gamble Manufacturing Company
84126-107
TOPICAL
0.35 g in 100 mL
3/19/2025
ABC Compounding Co., Inc.
62257-160
TOPICAL
3 mg in 1 mL
4/22/2025
BLANSETT PHARMACAL CO
51674-0117
TOPICAL
1 mg in 1 mL
3/20/2017
Royal Paper Corp.
59723-101
TOPICAL
1 g in 1 L
8/22/2024
KYNC DESIGN LLC
76557-050
CUTANEOUS, TOPICAL
0.2 g in 100 g
5/20/2025
ABC Compounding Co., Inc.
62257-875
TOPICAL
3 mg in 1 mL
4/22/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
ANTIMICROBIAL LOTION CREAM SOAP
gojo industries, inc.
02020351
Soap Bar ,  Liquid - Topical
.6 %
12/31/1993
GERMICIDAL HAND SOAP LIQ 0.6%
ostrem chemical co ltd.
01977873
Liquid - Topical
0.6 %
12/31/1992
FOAMING HAND WASH
cp industries ltd
02366428
Solution - Topical (Commercial)
0.50 %
N/A
E-Z SCRUB ANTIMICROBIAL FOAM SOLUTION CONTAINING 3% PCMX
becton dickinson
02241055
Liquid - Topical
3 %
10/19/2000
GARD 0.5%
avmor ltd
00553557
Liquid - Topical
.5 %
12/31/1982
ABSORBINE JR LINIMENT
bridges consumer healthcare llc
01942301
Solution - Topical
0.5 %
12/31/1993
DETTOL LIQ 10%
safetex products ltd.
00310999
Liquid - Topical
10 %
12/31/1964
ANTISEPTIC LOTION SOAP
inland/alcare
00664529
Soap Bar - Topical
0.36 %
12/31/1986
ZETAR SHAMPOO
rhone-poulenc rorer consumer inc.
01937642
Shampoo ,  Liquid - Topical
0.5 %
12/31/1993
VIONEXUS ANTIMICROBIAL FOAMING SOAP
metrex research, llc
02244129
Liquid - Topical
1 %
6/8/2001

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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