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PROVON Antimicrobial Ltn Sp with 0.3% PCMX

Medically reviewed on September 15, 2017.

Dosage form: liquid
Ingredients: Chloroxylenol 0.003mg in 1mL
Labeler: GOJO Industries, Inc.
NDC Code: 21749-750

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

PROVON Antimicrobial Lotion Soap with 0.3% PCMX

Active ingredient

Chloroxylenol 0.3%

Purpose

Antimicrobial

Use

• Handwash to help decrease bacteria on the skin

• Recommended for repeated use

Warnings

For external use only

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

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

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

Directions

• Wet hands

• Apply a small amount of product and work into a lather

• Rinse well and dry hands completely

Inactive ingredients

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, Hydroxypropyl Methylcellulose, Fragrance (Parfum)

PROVON ANTIMICROBIAL LTN SP WITH 0.3% PCMX 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-750
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Chloroxylenol (CHLOROXYLENOL) Chloroxylenol0.003 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Coconut Acid 
Oleic Acid 
Sodium Sulfate 
MONOETHANOLAMINE 
COCO MONOETHANOLAMIDE 
Coco-Betaine 
Propylene Glycol 
VITAMIN A PALMITATE 
EDETATE SODIUM 
.ALPHA.-TOCOPHEROL ACETATE 
CORN OIL 
HYPROMELLOSE, UNSPECIFIED 
Packaging
#Item CodePackage Description
1NDC:21749-750-04118 mL in 1 BOTTLE
2NDC:21749-750-08236 mL in 1 BOTTLE
3NDC:21749-750-12355 mL in 1 BOTTLE
4NDC:21749-750-16473 mL in 1 BOTTLE
5NDC:21749-750-50500 mL in 1 BOTTLE
6NDC:21749-750-80800 mL in 1 BOTTLE
7NDC:21749-750-101000 mL in 1 BAG
8NDC:21749-750-202000 mL in 1 BOTTLE
9NDC:21749-750-373784 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/31/2013
Labeler - GOJO Industries, Inc. (004162038)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.036424534manufacture(21749-750)
Establishment
NameAddressID/FEIOperations
GOJO Industries, Inc.088312414label(21749-750), pack(21749-750)

 
GOJO Industries, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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