Bayer Rapid Relief Powder
NDC Package 0280-0103-01

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

Package Information

Bayer Rapid Relief (aspirin/caffeine oral powder) powders is adults and children 12 years and over: take contents of 1 powder pack every 6 hours. This formulation utilizes a powder delivery system. Marketed by Bayer Healthcare Llc., this product is identified by NDC 0280-0103 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
0280-0103-01
Package Description
1 PACKET in 1 CARTON / 10 POWDER in 1 PACKET
Product Code
11-Digit Billing Format
00280010301
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Bayer Rapid Relief
Non-Proprietary Name
Aspirin/caffeine Oral Powder
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 and over: take contents of 1 powder pack every 6 hours. Dissolve powder on tongue, followed by a full glass of water. Do not exceed 4 powder packs in 24 hours. ● children under 12 years: consult a doctor

Regulatory & Marketing

Labeler Name
Bayer Healthcare Llc.
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-13-2023
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0280-0103). Click a package code to view its specific billing and regulatory data.

1 PACKET in 1 CARTON / 20 POWDER in 1 PACKET
1 PACKET in 1 CARTON / 30 POWDER in 1 PACKET

* 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 0280-0103-01 identifies a specific commercial package of 1 packet in 1 carton / 10 powder in 1 packet of Bayer Rapid Relief, a human over the counter drug labeled by Bayer Healthcare Llc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 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 Bayer Healthcare Llc. on January 13, 2023. The current certification is valid through December 31, 2026.

How is this Bayer Healthcare Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00280010301. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 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 (4-4-2)
0280-0103-01
11-Digit CMS (5-4-2)
00280-0103-01

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