Neomen Antifungal Pen Liquid
NDC Package 88017-001-01

11-digit billing NDC: 88017000101

Package Information

Neomen Antifungal Pen (undecylenic acid) liquids is wash the affected area and dry thoroughlyapply a thin layer over affected area twice daily (morning and night)supervise children in the use of this productfor athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks; if condition persists longer, ask a doctorthis product is not effective on the scalp or nails. This formulation utilizes a liquid delivery system. Marketed by Heartland Cloud Llc, this product is identified by NDC 88017-001 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
88017-001-01
Package Description
4 APPLICATOR in 1 BOX / 3 mL in 1 APPLICATOR
Product Code
11-Digit Billing Format
88017000101

Clinical Specifications

Proprietary Name
Neomen Antifungal Pen
Non-Proprietary Name
Undecylenic Acid
Substance Name
Undecylenic Acid
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
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)
Usage Information
Wash the affected area and dry thoroughlyapply a thin layer over affected area twice daily (morning and night)supervise children in the use of this productfor athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete's foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks; if condition persists longer, ask a doctorthis product is not effective on the scalp or nails

Regulatory & Marketing

Labeler Name
Heartland Cloud Llc
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-22-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 88017-001-01 identifies a specific commercial package of 4 applicator in 1 box / 3 ml in 1 applicator of Neomen Antifungal Pen, a human over the counter drug labeled by Heartland Cloud Llc. This liquid is formulated for topical use and contains undecylenic acid as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Heartland Cloud Llc on September 22, 2026. The current certification is valid through December 31, 2027.

How is this Heartland Cloud Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 88017000101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
88017-001-01
11-Digit CMS (5-4-2)
88017-0001-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.