Axim Night Time - Liquid
NDC Package 82706-012-01

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

Package Information

Axim Night Time - Liquid (acetaminophen, dextromethorphan hydrobromide, doxylamine succinate) liquids is take only as directed (see overdose warning)measure only with dosage cup provided and keep dosage cup with productmL = milliliterdo not exceed 4 doses per 24 hourswhen using DayTime and NightTime products, limit total to 4 doses per 24 hoursadults and children 12 years and over30 mL every 6 hourschildren under 12 yearsdo not use. This formulation utilizes a liquid delivery system. Marketed by Vivunt Pharma Llc, this product is identified by NDC 82706-012 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
82706-012-01
Package Description
355 mL in 1 BOTTLE, PLASTIC
Product Code
82706-012
11-Digit Billing Format
82706001201
RxNorm Crosswalk
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 30 mL Oral Solution
  • RxCUI: 1043400 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG per 15 ML Oral Solution
  • RxCUI: 1043400 - acetaminophen 650 MG / dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG per 30 ML Oral Solution
  • RxCUI: 1043400 - APAP 21.7 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Axim Night Time - Liquid
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Doxylamine Succinate
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Take only as directed (see overdose warning)measure only with dosage cup provided and keep dosage cup with productmL = milliliterdo not exceed 4 doses per 24 hourswhen using DayTime and NightTime products, limit total to 4 doses per 24 hoursadults and children 12 years and over30 mL every 6 hourschildren under 12 yearsdo 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
01-05-2024
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 82706-012-01 identifies a specific commercial package of 355 ml in 1 bottle, plastic of Axim Night Time - Liquid, a human over the counter drug labeled by Vivunt Pharma Llc. This liquid is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; doxylamine succinate 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 January 05, 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: 82706001201. 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)
82706-012-01
11-Digit CMS (5-4-2)
82706-0012-01

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