Midol Complete Tablet
NDC Package 85237-1841-2

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

Package Information

Midol Complete (acetaminophen, caffeine, and pyrilamine maleate) tablets is do not take more than the recommended doseadults and children 12 years and older: take 2 caplets with waterrepeat every 6 hours, as neededdo not exceed 6 caplets per daychildren under 12 years: consult a doctor. This formulation utilizes a tablet delivery system. Marketed by Select Consumer Group, this product is identified by NDC 85237-1841 and is authorized under FDA application M027.

Identification & Billing

NDC Package Code
85237-1841-2
Package Description
2 POUCH in 1 BLISTER PACK / 2 TABLET in 1 POUCH
Product Code
11-Digit Billing Format
85237184102
RxNorm Crosswalk
  • RxCUI: 1597298 - acetaminophen 500 MG / caffeine 60 MG / pyrilamine maleate 15 MG Oral Tablet
  • RxCUI: 1597298 - APAP 500 MG / Caffeine 60 MG / Pyrilamine Maleate 15 MG Oral Tablet

Clinical Specifications

Proprietary Name
Midol Complete
Non-Proprietary Name
Acetaminophen, Caffeine, And Pyrilamine Maleate
Substance Name
Acetaminophen; Caffeine; Pyrilamine Maleate
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Do not take more than the recommended doseadults and children 12 years and older: take 2 caplets with waterrepeat every 6 hours, as neededdo not exceed 6 caplets per daychildren under 12 years: consult a doctor

Regulatory & Marketing

Labeler Name
Select Consumer Group
Product Type
Human Otc Drug
FDA Application #
M027
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-10-2014
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 (85237-1841). Click a package code to view its specific billing and regulatory data.

1 POUCH in 1 BLISTER PACK / 2 TABLET in 1 POUCH
20 POUCH in 1 BOX, UNIT-DOSE / 2 TABLET in 1 POUCH
25 POUCH in 1 BOX, UNIT-DOSE / 2 TABLET in 1 POUCH
30 POUCH in 1 BOX, UNIT-DOSE / 2 TABLET in 1 POUCH

* 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 85237-1841-2 identifies a specific commercial package of 2 pouch in 1 blister pack / 2 tablet in 1 pouch of Midol Complete, a human over the counter drug labeled by Select Consumer Group. This tablet is formulated for oral use and contains acetaminophen; caffeine; pyrilamine maleate 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 Select Consumer Group on February 10, 2014. The current certification is valid through December 31, 2026.

How is this Select Consumer Group product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85237184102. 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 (5-4-1)
85237-1841-2
11-Digit CMS (5-4-2)
85237-1841-02

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