Goodsense Medicated Pads
NDC Package 75981-007-47

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 inactivated by the FDA.

Goodsense Medicated Pads is directionsAs hemorrhoidal treatment for adults:When practical clean the affected area with mild soap and warm water and rinse thoroughlyGently dry by patting or blotting with toilet tissue or soft cloth before applyingGently apply to the affected area by patting and then discardCan be used up to six times daily or after each bowel movementChildren under 12 years of age: ask a doctor. Marketed by Geiss, Destin And Dunn, Inc., this product is identified by NDC 75981-007 and is authorized under FDA application part346.

Identification & Billing

NDC Package Code
75981-007-47
Package Description
100 APPLICATOR in 1 JAR / 2.5 mL in 1 APPLICATOR
Product Code
75981-007
11-Digit Billing Format
75981000747
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Goodsense Medicated Pads
Dosage Form
-
Usage Information
DirectionsAs hemorrhoidal treatment for adults:When practical clean the affected area with mild soap and warm water and rinse thoroughlyGently dry by patting or blotting with toilet tissue or soft cloth before applyingGently apply to the affected area by patting and then discardCan be used up to six times daily or after each bowel movementChildren under 12 years of age: ask a doctor

Regulatory & Marketing

Labeler Name
Geiss, Destin And Dunn, Inc.
FDA Application #
part346
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-01-2011
Listing Expiration
12-31-2018
Exclude Flag
I
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 75981-007-47 identifies a specific commercial package of 100 applicator in 1 jar / 2.5 ml in 1 applicator of Goodsense Medicated Pads, labeled by Geiss, Destin And Dunn, 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 Geiss, Destin And Dunn, Inc. on June 01, 2011. The current certification is valid through December 31, 2018.

How is this Geiss, Destin And Dunn, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 75981000747. 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)
75981-007-47
11-Digit CMS (5-4-2)
75981-0007-47

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