Publix Extra Strength
NDC Package 41415-200-96

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Publix Extra Strength is •adults and children 12 years of age and over: chew 2-4 tablets completely as symptoms occur, or as directed by a doctor.•do not take for symptoms that persist for more than 2 weeks unless advised by a doctor. Marketed by Publix Super Markets, Inc, this product is identified by NDC 41415-200 and is authorized under FDA application part331.

Identification & Billing

NDC Package Code
41415-200-96
Package Description
96 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product Code
41415-200
11-Digit Billing Format
41415020096
RxNorm Crosswalk
  • RxCUI: 308915 - calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet
  • RxCUI: 308915 - calcium carbonate 750 MG Chewable Tablet
  • RxCUI: 308915 - calcium carbonate 750 MG (calcium 300 MG) Chewable Tablet

Clinical Specifications

Proprietary Name
Publix Extra Strength Assorted Fruit
Dosage Form
-
Usage Information
•adults and children 12 years of age and over: chew 2-4 tablets completely as symptoms occur, or as directed by a doctor.•do not take for symptoms that persist for more than 2 weeks unless advised by a doctor.

Regulatory & Marketing

Labeler Name
Publix Super Markets, Inc
FDA Application #
part331
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
05-21-2019
Listing Expiration
12-31-2022
Exclude Flag
I
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 41415-200-96 identifies a specific commercial package of 96 tablet, chewable in 1 bottle, plastic of Publix Extra Strength Assorted Fruit, labeled by Publix Super Markets, Inc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Publix Super Markets, Inc on May 21, 2019. The current certification is valid through December 31, 2022.

How is this Publix Super Markets, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41415020096. 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)
41415-200-96
11-Digit CMS (5-4-2)
41415-0200-96

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