Otis Clapp Mygrex
NDC Package 47682-148-99

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Otis Clapp Mygrex is ■ do not use more than directedAdults and children: (12 years and older) Take 2 tablets every 6 hours. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-148 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
47682-148-99
Package Description
2 TABLET in 1 PACKET
Product Code
47682-148
11-Digit Billing Format
47682014899
RxNorm Crosswalk
  • RxCUI: 1101534 - acetaminophen 500 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1101534 - acetaminophen 500 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1101534 - APAP 500 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet

Clinical Specifications

Proprietary Name
Otis Clapp Mygrex
Dosage Form
-
Usage Information
■ do not use more than directedAdults and children: (12 years and older) Take 2 tablets every 6 hours. Do not take more than 8 tablets in 24 hours. Children under 12 years: Do not give this adult strength product to children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.

Regulatory & Marketing

Labeler Name
Unifirst First Aid Corporation
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-30-2008
Listing Expiration
12-31-2023
Exclude Flag
I
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 (47682-148). Click a package code to view its specific billing and regulatory data.

47682-148-03
150 PACKET in 1 BOX / 2 TABLET in 1 PACKET (47682-148-99)

* 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 47682-148-99 identifies a specific commercial package of 2 tablet in 1 packet of Otis Clapp Mygrex, labeled by Unifirst First Aid Corporation. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Unifirst First Aid Corporation on December 30, 2008. The current certification is valid through December 31, 2023.

How is this Unifirst First Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 47682014899. 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)
47682-148-99
11-Digit CMS (5-4-2)
47682-0148-99

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