Quality Choice Pain Relief Powder
NDC Package 63868-661-50

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

Package Information

Quality Choice Pain Relief Powder (aspirin and caffeine) powders is adults and children 12 years of age and over: place 1 powder on tongue every 6 hours, while symptoms persist. This formulation utilizes a powder delivery system. Marketed by Chain Drug Marketing Association, this product is identified by NDC 63868-661 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
63868-661-50
Package Description
50 PACKET in 1 CARTON / 1 POWDER in 1 PACKET
Product Code
11-Digit Billing Format
63868066150
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
50 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Quality Choice Pain Relief Powder
Non-Proprietary Name
Aspirin And Caffeine
Substance Name
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)
Usage Information
Adults and children 12 years of age and over: place 1 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 powders in 24 hours unless directed by a doctor.children under 12 years of age: ask a doctor.

Regulatory & Marketing

Labeler Name
Chain Drug Marketing Association
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-25-2021
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 63868-661-50 identifies a specific commercial package of 50 packet in 1 carton / 1 powder in 1 packet of Quality Choice Pain Relief Powder, a human over the counter drug labeled by Chain Drug Marketing Association. 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 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 Chain Drug Marketing Association on March 25, 2021. The current certification is valid through December 31, 2026.

How is this Chain Drug Marketing Association product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63868066150. 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)
63868-661-50
11-Digit CMS (5-4-2)
63868-0661-50

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