Miconazole Nitrate
NDC Package 69367-399-85

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Miconazole Nitrate is clean the affected area and dry thoroughlyapply a thin layer of powder over affected area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot, pay special attention to spaces between toes; wear well - fitting, ventilated shoes, and change shoes and socks at least once dailyfor athletes foot and ringworm, use daily for 4 weeksfor jock itch, use daily for 2 weeksif condition persists longer, consult a doctorthis product is not effective on the scalp or nails. Marketed by Westminster Pharmaceuticals, Llc, this product is identified by NDC 69367-399 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
69367-399-85
Package Description
85 g in 1 BOTTLE
Product Code
69367-399
11-Digit Billing Format
69367039985

Clinical Specifications

Proprietary Name
Miconazole Nitrate
Dosage Form
-
Usage Information
Clean the affected area and dry thoroughlyapply a thin layer of powder over affected area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot, pay special attention to spaces between toes; wear well - fitting, ventilated shoes, and change shoes and socks at least once dailyfor athletes foot and ringworm, use daily for 4 weeksfor jock itch, use daily for 2 weeksif condition persists longer, consult a doctorthis product is not effective on the scalp or nails

Regulatory & Marketing

Labeler Name
Westminster Pharmaceuticals, Llc
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-16-2024
End Marketing Date
05-01-2026
Listing Expiration
05-01-2026
Exclude Flag
D
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 69367-399-85 identifies a specific commercial package of 85 g in 1 bottle of Miconazole Nitrate, labeled by Westminster Pharmaceuticals, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Westminster Pharmaceuticals, Llc on May 16, 2024. The current certification is valid through May 01, 2026.

How is this Westminster Pharmaceuticals, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69367039985. 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)
69367-399-85
11-Digit CMS (5-4-2)
69367-0399-85

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