Cherry Antacid Soft Chews
NDC Package 75981-010-36

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.

Cherry Antacid Soft Chews is uses: Relievesheartburnsour stomachacid indigestionupset stomach due to these symptoms. Marketed by Geiss, Destin, & Dunn, this product is identified by NDC 75981-010 and is authorized under FDA application part331.

Identification & Billing

NDC Package Code
75981-010-36
Package Description
36 TABLET, CHEWABLE in 1 BAG
Product Code
75981-010
11-Digit Billing Format
75981001036
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Cherry Antacid Soft Chews
Dosage Form
-
Usage Information
Uses: Relievesheartburnsour stomachacid indigestionupset stomach due to these symptoms

Regulatory & Marketing

Labeler Name
Geiss, Destin, & Dunn
FDA Application #
part331
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-04-2012
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 75981-010-36 identifies a specific commercial package of 36 tablet, chewable in 1 bag of Cherry Antacid Soft Chews, labeled by Geiss, Destin, & Dunn. 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 Geiss, Destin, & Dunn on June 04, 2012. The current certification is valid through December 31, 2022.

How is this Geiss, Destin, & Dunn product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 75981001036. 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)
75981-010-36
11-Digit CMS (5-4-2)
75981-0010-36

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