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  5. NDC Package Code: 61924-093-34 Kleenfoam

NDC Package 61924-093-34 Kleenfoam

Otc Antimicrobial Drug Product Aerosol, Foam Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
61924-093-34
Package Description:
1000 mL in 1 CARTRIDGE
Product Code:
61924-093
Proprietary Name:
Kleenfoam
Non-Proprietary Name:
Otc Antimicrobial Drug Product
Substance Name:
Chloroxylenol
Usage Information:
Wet hands and forearms.Apply 5 millimeters (teaspoon) or palmful to hands and forearms.Scrub thoroughly for 15 seconds.Rinse and repeat.
11-Digit NDC Billing Format:
61924009334
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Dermarite Industries Llc
Dosage Form:
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
CHLOROXYLENOL .005 g/mL
Sample Package:
No
FDA Application Number:
M003
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-12-2011
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 61924-093-34?

The NDC Packaged Code 61924-093-34 is assigned to a package of 1000 ml in 1 cartridge of Kleenfoam, a human over the counter drug labeled by Dermarite Industries Llc. The product's dosage form is aerosol, foam and is administered via topical form.

Is NDC 61924-093 included in the NDC Directory?

Yes, Kleenfoam with product code 61924-093 is active and included in the NDC Directory. The product was first marketed by Dermarite Industries Llc on December 12, 2011 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 61924-093-34?

The 11-digit format is 61924009334. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-261924-093-345-4-261924-0093-34