NDC Package 63868-020-08 Daytime Cold And Flu Non Drowsy

Acetaminophen,Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

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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:

63868-020-08

Package Description:

237 mL in 1 BOTTLE, PLASTIC

Product Code:

63868-020

Proprietary Name:

Daytime Cold And Flu Non Drowsy

Non-Proprietary Name:

Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride

Substance Name:

Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride

Usage Information:

Do not take more than directed (see overdose warning)do not exceed 4 doses in any 24-hour periodmeasure only with dosing cup provided. Do not use any other dosing devicekeep dosing cup with productmL=milliliteradults and children 12 years and over30 mL every 4 hours children 6 to under 12 years 15 mL every 4 hours children 4 to under 6 years ask a doctor children under 4 years do not use When using Day Time and Night Time products, carefully read each label to ensure correct dosing

11-Digit NDC Billing Format:

63868002008

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

237 ML

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:

Quality Choice (chain Drug Marketing Association)

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.

Active Ingredient(s):

ACETAMINOPHEN 325 mg/15mL

DEXTROMETHORPHAN HYDROBROMIDE 10 mg/15mL

PHENYLEPHRINE HYDROCHLORIDE 5 mg/15mL

Pharmacologic Class(es):

Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)

Sigma-1 Agonist - [EPC] (Established Pharmacologic Class)

Sigma-1 Receptor Agonists - [MoA] (Mechanism of Action)

Uncompetitive N-methyl-D-aspartate Receptor Antagonist - [EPC] (Established Pharmacologic Class)

Uncompetitive NMDA Receptor Antagonists - [MoA] (Mechanism of Action)

alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)

Sample Package:

FDA Application Number:

part341

Marketing Category:

OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.

Start Marketing Date:

06-30-2015

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

63868 - Quality Choice (chain Drug Marketing Association)
- 63868-020 - Daytime Cold And Flu
  - 63868-020-08 - 237 mL in 1 BOTTLE, PLASTIC

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 Code	Package Description
63868-020-12	355 mL in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 63868-020-08?

The NDC Packaged Code 63868-020-08 is assigned to a package of 237 ml in 1 bottle, plastic of Daytime Cold And Flu Non Drowsy, a human over the counter drug labeled by Quality Choice (chain Drug Marketing Association). The product's dosage form is liquid and is administered via oral form.This product is billed per "ML" milliliter and contains an estimated amount of 237 billable units per package.

Is NDC 63868-020 included in the NDC Directory?

Yes, Daytime Cold And Flu Non Drowsy with product code 63868-020 is active and included in the NDC Directory. The product was first marketed by Quality Choice (chain Drug Marketing Association) on June 30, 2015 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 NDC billing unit for package 63868-020-08?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 237.

What is the 11-digit format for NDC 63868-020-08?

The 11-digit format is 63868002008. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	63868-020-08	5-4-2	63868-0020-08

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