Vicks Nyquil Kids Berry Liquid
NDC Package 69423-779-08

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

Package Information

Vicks Nyquil Kids Berry (chlorpheniramine maleate, dextromethorphan hbr) liquids is • take only as directed • only use the dose cup provided • do not exceed 4 doses per 24 hrs adults & children 12 yrs & over30 mL every 6 hrschildren 6 to under 12 yrs15 mL every 6 hrschildren 4 to under 6 yrsdo not use unless directed by a doctorchildren under 4 yrsdo not use • take only as directed • only use the dose cup provided • do not exceed 4 doses per 24 hrs adults & children 12 yrs & over30 mL every 4 hrschildren 6 to under 12 yrs15 mL every 4 hrschildren 4 to under 6 yrsask a doctorchildren under 4 yrsdo not use. This formulation utilizes a liquid delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 69423-779 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
69423-779-08
Package Description
236 mL in 1 BOTTLE, PLASTIC
Product Code
69423-779
11-Digit Billing Format
69423077908
RxNorm Crosswalk
  • RxCUI: 1114361 - chlorpheniramine maleate 2 MG / dextromethorphan HBr 15 MG in 15 mL Oral Solution
  • RxCUI: 1114361 - chlorpheniramine maleate 0.133 MG/ML / dextromethorphan hydrobromide 1 MG/ML Oral Solution
  • RxCUI: 1114361 - chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG per 15 ML Oral Solution
  • RxCUI: 2566816 - dextromethorphan HBr 10 MG / guaiFENesin 100 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 2566816 - dextromethorphan hydrobromide 0.667 MG/ML / guaifenesin 6.667 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Vicks Nyquil Kids Berry Cold And Cough Plus Runny Nose
Non-Proprietary Name
Chlorpheniramine Maleate, Dextromethorphan Hbr
Substance Name
Chlorpheniramine Maleate; Dextromethorphan Hydrobromide
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 • only use the dose cup provided • do not exceed 4 doses per 24 hrs adults & children 12 yrs & over30 mL every 6 hrschildren 6 to under 12 yrs15 mL every 6 hrschildren 4 to under 6 yrsdo not use unless directed by a doctorchildren under 4 yrsdo not use • take only as directed • only use the dose cup provided • do not exceed 4 doses per 24 hrs adults & children 12 yrs & over30 mL every 4 hrschildren 6 to under 12 yrs15 mL every 4 hrschildren 4 to under 6 yrsask a doctorchildren under 4 yrsdo not use

Regulatory & Marketing

Labeler Name
The Procter & Gamble Manufacturing Company
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-06-2023
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 69423-779-08 identifies a specific commercial package of 236 ml in 1 bottle, plastic of Vicks Nyquil Kids Berry Cold And Cough Plus Runny Nose, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. This liquid is formulated for oral use and contains chlorpheniramine maleate; dextromethorphan hydrobromide 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 The Procter & Gamble Manufacturing Company on June 06, 2023. The current certification is valid through December 31, 2026.

How is this The Procter & Gamble Manufacturing Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69423077908. 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)
69423-779-08
11-Digit CMS (5-4-2)
69423-0779-08

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