Proski Benzo
NDC Package 84289-216-20

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.

Proski Benzo is sensitivity Test for a New User. Marketed by Pharmamed Usa Inc, this product is identified by NDC 84289-216 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
84289-216-20
Package Description
1 TUBE in 1 CARTON / 20 g in 1 TUBE
Product Code
84289-216
11-Digit Billing Format
84289021620

Clinical Specifications

Proprietary Name
Proski Benzo
Dosage Form
-
Usage Information
Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below. clean the skin thoroughly before applying this product cover the entire affected area with a thin layer one to three times daily because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Regulatory & Marketing

Labeler Name
Pharmamed Usa Inc
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2025
End Marketing Date
05-21-2026
Listing Expiration
05-21-2026
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 84289-216-20 identifies a specific commercial package of 1 tube in 1 carton / 20 g in 1 tube of Proski Benzo, labeled by Pharmamed Usa Inc. 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 Pharmamed Usa Inc on April 01, 2025. The current certification is valid through May 21, 2026.

How is this Pharmamed Usa Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84289021620. 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)
84289-216-20
11-Digit CMS (5-4-2)
84289-0216-20

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