Goodys Extra Strength Powder
NDC Package 63029-644-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Goodys Extra Strength (acetaminophen, aspirin, and caffeine) powders is do not take more than directed (see overdose warning)adults and children 12 years and over: place 1 powder on tongue every 6 hours, while symptoms persist. This formulation utilizes a powder delivery system. Marketed by Medtech Products Inc., this product is identified by NDC 63029-644 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
63029-644-01
Package Description
50 POWDER in 1 BOX
Product Code
11-Digit Billing Format
63029064401
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
50 EA
RxNorm Crosswalk
  • RxCUI: 763116 - acetaminophen 260 MG / aspirin 520 MG / caffeine 32.5 MG Oral Powder
  • RxCUI: 763116 - APAP 260 MG / ASA 520 MG / Caffeine 32.5 MG Oral Powder

Clinical Specifications

Proprietary Name
Goodys Extra Strength
Non-Proprietary Name
Acetaminophen, Aspirin, And Caffeine
Substance Name
Acetaminophen; Aspirin; Caffeine
Dosage Form
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Do not take more than directed (see overdose warning)adults and children 12 years and over: place 1 powder on tongue every 6 hours, while symptoms persist. Drink a full glass of water with each dose, or stir powder into a glass of water or other liquid. do not take more than 4 powders in 24 hours unless directed by a doctor. children under 12 years of age: ask a doctor.

Regulatory & Marketing

Labeler Name
Medtech Products Inc.
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-01-2013
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 63029-644-01 identifies a specific commercial package of 50 powder in 1 box of Goodys Extra Strength, a human over the counter drug labeled by Medtech Products Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 50 billable units per package. This powder is formulated for oral use and contains acetaminophen; aspirin; caffeine 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 Medtech Products Inc. on November 01, 2013. The current certification is valid through December 31, 2026.

How is this Medtech Products Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63029064401. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 50 total billable units per package. 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)
63029-644-01
11-Digit CMS (5-4-2)
63029-0644-01

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