Noorish Foot Co. Anti-fungal Pen Liquid
NDC Package 84841-111-11

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Noorish Foot Co. Anti-fungal Pen (anti-fungal pen) liquids is • Wash the affected area and dry thoroughly. This formulation utilizes a liquid delivery system. Marketed by Noorish Foot Co. Llc, this product is identified by NDC 84841-111 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
84841-111-11
Package Description
2 APPLICATOR in 1 BOX / 5 mL in 1 APPLICATOR
Product Code
84841-111
11-Digit Billing Format
84841011111

Clinical Specifications

Proprietary Name
Noorish Foot Co. Anti-fungal Pen
Non-Proprietary Name
Anti-fungal Pen
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)
UNDECYLENIC ACID 10 mg/100mL
Usage Information
• Wash the affected area and dry thoroughly. • Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. • Supervise children in the use of this product. • For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily • For athlete's foot and ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor.

Regulatory & Marketing

Labeler Name
Noorish Foot Co. Llc
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2025
Listing Expiration
12-31-2026
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 84841-111-11 identifies a specific commercial package of 2 applicator in 1 box / 5 ml in 1 applicator of Noorish Foot Co. Anti-fungal Pen, a human over the counter drug labeled by Noorish Foot Co. 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 Noorish Foot Co. Llc on January 01, 2025. The current certification is valid through December 31, 2026.

How is this Noorish Foot Co. Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84841011111. 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)
84841-111-11
11-Digit CMS (5-4-2)
84841-0111-11

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