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  5. NDC Package Code: 50804-207-03 Arthritis Relief Goodsense

NDC Package 50804-207-03 Arthritis Relief Goodsense

Trolamine Salicylate Cream Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50804-207-03
Package Description:
1 TUBE in 1 CARTON / 85 g in 1 TUBE
Product Code:
50804-207
Proprietary Name:
Arthritis Relief Goodsense
Non-Proprietary Name:
Trolamine Salicylate
Substance Name:
Trolamine Salicylate
Usage Information:
Adults and children over 12 years: apply generously to the affected area, massage into painful area until thoroughly absorbed into the skin, repeat as necessary, but no more than 4 times daily. Children under 12 years or younger: ask a doctor.
11-Digit NDC Billing Format:
50804020703
Product Type:
Human Otc Drug
Labeler Name:
Geiss, Destin & Dunn, Inc
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
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):
TROLAMINE SALICYLATE 10 g/100g
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-01-2019
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 50804-207-03?

The NDC Packaged Code 50804-207-03 is assigned to a package of 1 tube in 1 carton / 85 g in 1 tube of Arthritis Relief Goodsense, a human over the counter drug labeled by Geiss, Destin & Dunn, Inc. The product's dosage form is cream and is administered via topical form.

Is NDC 50804-207 included in the NDC Directory?

Yes, Arthritis Relief Goodsense with product code 50804-207 is active and included in the NDC Directory. The product was first marketed by Geiss, Destin & Dunn, Inc on November 01, 2019 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 50804-207-03?

The 11-digit format is 50804020703. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-250804-207-035-4-250804-0207-03