Night Time Severe Cold And Cough Relief Liquid
NDC Package 68016-154-08

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

Package Information

Night Time Severe Cold And Cough Relief (acetaminophen, diphenhydramine hcl, phenylephrine hcl) liquids is age                                                                                  DoseChildren under 4 years                                                      Do not useChildren 4 to under 12 years of age                                    Do not use unless directed by a doctorAdults and children 12 years and over                                2 tablespoonful (30 mL) every 4 hourstake only as recommended (see Overdose warning)use dose cup or tablespoon (TBSP)do not take more than 6 doses in any 24-hour period. This formulation utilizes a liquid delivery system. Marketed by Chain Drug Consortium, Llc, this product is identified by NDC 68016-154 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
68016-154-08
Package Description
245 mL in 1 BOTTLE
Product Code
68016-154
11-Digit Billing Format
68016015408
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
245 ML
RxNorm Crosswalk
  • RxCUI: 1298348 - acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 1298348 - acetaminophen 21.7 MG/ML / diphenhydramine hydrochloride 0.833 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • RxCUI: 1298348 - acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
  • RxCUI: 1298348 - acetaminophen 650 MG / diphenhydramine HCl 25 MG / phenylephrine HCl 10 MG per 30 ML Oral Solution
  • RxCUI: 1298348 - APAP 21.7 MG/ML / Diphenhydramine Hydrochloride 0.833 MG/ML / Phenylephrine Hydrochloride 0.333 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Night Time Severe Cold And Cough Relief
Non-Proprietary Name
Acetaminophen, Diphenhydramine Hcl, Phenylephrine Hcl
Substance Name
Acetaminophen; Diphenhydramine Hydrochloride; Phenylephrine Hydrochloride
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
Age                                                                                  DoseChildren under 4 years                                                      Do not useChildren 4 to under 12 years of age                                    Do not use unless directed by a doctorAdults and children 12 years and over                                2 tablespoonful (30 mL) every 4 hourstake only as recommended (see Overdose warning)use dose cup or tablespoon (TBSP)do not take more than 6 doses in any 24-hour period

Regulatory & Marketing

Labeler Name
Chain Drug Consortium, Llc
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-04-2013
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 68016-154-08 identifies a specific commercial package of 245 ml in 1 bottle of Night Time Severe Cold And Cough Relief, a human over the counter drug labeled by Chain Drug Consortium, Llc. This liquid is formulated for oral use and contains acetaminophen; diphenhydramine hydrochloride; phenylephrine 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 Chain Drug Consortium, Llc on October 04, 2013. The current certification is valid through December 31, 2026.

How is this Chain Drug Consortium, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68016015408. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 245 total billable units per package. 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)
68016-154-08
11-Digit CMS (5-4-2)
68016-0154-08

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