Notts - Pain Relief Pm Tablet
NDC Package 82706-009-01

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

Notts - Pain Relief Pm (acetaminophen, diphenhydramine hydrochloride) tablets is do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets at bedtime if needed, or as directed by a doctor.do not take more than 2 caplets in 24 hourschildren under 12 yearsdo not use. This formulation utilizes a tablet delivery system. Marketed by Vivunt Pharma Llc, this product is identified by NDC 82706-009 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
82706-009-01
Package Description
1 BOTTLE in 1 CARTON / 24 TABLET in 1 BOTTLE
Product Code
82706-009
11-Digit Billing Format
82706000901
RxNorm Crosswalk
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet

Clinical Specifications

Proprietary Name
Notts - Pain Relief Pm
Non-Proprietary Name
Acetaminophen, Diphenhydramine Hydrochloride
Substance Name
Acetaminophen; Diphenhydramine Hydrochloride
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.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 caplets at bedtime if needed, or as directed by a doctor.do not take more than 2 caplets in 24 hourschildren under 12 yearsdo not use

Regulatory & Marketing

Labeler Name
Vivunt Pharma Llc
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-17-2022
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 (82706-009). Click a package code to view its specific billing and regulatory data.

82706-009-02
1 BOTTLE in 1 CARTON / 50 TABLET in 1 BOTTLE

* 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 82706-009-01 identifies a specific commercial package of 1 bottle in 1 carton / 24 tablet in 1 bottle of Notts - Pain Relief Pm, a human over the counter drug labeled by Vivunt Pharma Llc. This tablet is formulated for oral use and contains acetaminophen; diphenhydramine hydrochloride 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 Vivunt Pharma Llc on August 17, 2022. The current certification is valid through December 31, 2026.

How is this Vivunt Pharma Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82706000901. 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)
82706-009-01
11-Digit CMS (5-4-2)
82706-0009-01

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