Drx Choice Capsule, Liquid Filled
NDC Package 68163-061-10

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

Package Information

Drx Choice (acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride) capsules is ▪take only as directed ▪do not exceed 8 softgels per 24 hrsadults & children 12 yrs & over2 softgels with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Raritan Pharmaceuticals Inc., this product is identified by NDC 68163-061 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
68163-061-10
Package Description
5 POUCH in 1 CARTON / 2 CAPSULE, LIQUID FILLED in 1 POUCH
Product Code
68163-061
11-Digit Billing Format
68163006110

Clinical Specifications

Proprietary Name
Drx Choice Daytime Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, And Phenylephrine Hydrochloride
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride
Dosage Form
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
▪take only as directed ▪do not exceed 8 softgels per 24 hrsadults & children 12 yrs & over2 softgels with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use

Regulatory & Marketing

Labeler Name
Raritan Pharmaceuticals Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2026
Listing Expiration
12-31-2027
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 68163-061-10 identifies a specific commercial package of 5 pouch in 1 carton / 2 capsule, liquid filled in 1 pouch of Drx Choice Daytime Cold And Flu, a human over the counter drug labeled by Raritan Pharmaceuticals Inc.. This capsule, liquid filled is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; 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 Raritan Pharmaceuticals Inc. on June 01, 2026. The current certification is valid through December 31, 2027.

How is this Raritan Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68163006110. 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)
68163-061-10
11-Digit CMS (5-4-2)
68163-0061-10

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