Axiv Allergy Relief Tablet
NDC Package 82706-021-02

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

Package Information

Axiv Allergy Relief (diphenhydramine hydrochloride) tablets is take every 4 to 6 hours, or as directed by a doctordo not take more than 12 caplets in 24 hours for adults and children 12 years and over. This formulation utilizes a tablet delivery system. Marketed by Vivunt Pharma Llc, this product is identified by NDC 82706-021 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
82706-021-02
Package Description
50 POUCH in 1 CARTON / 2 TABLET in 1 POUCH
Product Code
82706-021
11-Digit Billing Format
82706002102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Axiv Allergy Relief
Non-Proprietary Name
Diphenhydramine Hydrochloride
Substance Name
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)
DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Pharmacologic Class
Usage Information
Take every 4 to 6 hours, or as directed by a doctordo not take more than 12 caplets in 24 hours for adults and children 12 years and over. Do not take more than 6 caplets for children 6 to under 12 years of age in 24 hoursadults and children 12 years and over 1 or 2 caplets children 6 to under 12 years 1 capletchildren under 6 years do not use

Regulatory & Marketing

Labeler Name
Vivunt Pharma Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-09-2024
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 82706-021-02 identifies a specific commercial package of 50 pouch in 1 carton / 2 tablet in 1 pouch of Axiv Allergy Relief, a human over the counter drug labeled by Vivunt Pharma Llc. This tablet is formulated for oral use and contains 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 July 09, 2024. 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: 82706002102. 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)
82706-021-02
11-Digit CMS (5-4-2)
82706-0021-02

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