NDC Package 68016-236-08 Cold And Flu Day Time Multi-symptom Relief

Acetaminophen,Dextromethorphan Hbr,Phenylephrine Hcl Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
68016-236-08
Package Description:
237 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Cold And Flu Day Time Multi-symptom Relief
Non-Proprietary Name:
Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Usage Information:
Uses temporarily relieves these common cold/flu symptoms:• minor aches and pains • headache • sore throat • fever• nasal congestion • cough due to minor throat and bronchial irritation
11-Digit NDC Billing Format:
68016023608
NDC to RxNorm Crosswalk:
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 1113705 - acetaminophen 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
  • RxCUI: 1113705 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG per 30 ML Oral Solution
  • RxCUI: 1113705 - APAP 21.7 MG/ML / dextromethorphan hydrobromide 0.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Pharmacy Value Alliance, Llc
    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(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M012
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-01-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68016-236-12354 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68016-236-08?

    The NDC Packaged Code 68016-236-08 is assigned to a package of 237 ml in 1 bottle of Cold And Flu Day Time Multi-symptom Relief, a human over the counter drug labeled by Pharmacy Value Alliance, Llc. The product's dosage form is liquid and is administered via oral form.

    Is NDC 68016-236 included in the NDC Directory?

    Yes, Cold And Flu Day Time Multi-symptom Relief with product code 68016-236 is active and included in the NDC Directory. The product was first marketed by Pharmacy Value Alliance, Llc on October 01, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68016-236-08?

    The 11-digit format is 68016023608. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-268016-236-085-4-268016-0236-08