Goodys Powder
NDC Package 63029-668-16

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

Package Information

Goodys (acetaminophen, aspirin, and caffeine) powders is do not take more than directed (see overdose warning)adults and children 12 years and over: open 1 pack, place 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 63029-668 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
63029-668-16
Package Description
16 POWDER in 1 CARTON
Product Code
63029-668
11-Digit Billing Format
63029066816
RxNorm Crosswalk
  • RxCUI: 2734143 - acetaminophen 500 MG / aspirin 500 MG / caffeine 130 MG Oral Powder
  • RxCUI: 2734143 - APAP 500 MG / ASA 500 MG / caffeine 130 MG Oral Powder

Clinical Specifications

Proprietary Name
Goodys Max
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.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not take more than directed (see overdose warning)adults and children 12 years and over: open 1 pack, place powder on tongue every 6 hours, while symptoms persist. Drink a full glass of water with each dose or may stir powder into a glass of water or other liquid. do not take more than 4 packs 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
02-02-2026
Listing Expiration
12-31-2027
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 63029-668-16 identifies a specific commercial package of 16 powder in 1 carton of Goodys Max, a human over the counter drug labeled by Medtech Products Inc.. 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 February 02, 2026. The current certification is valid through December 31, 2027.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63029066816. 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)
63029-668-16
11-Digit CMS (5-4-2)
63029-0668-16

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