Ultra Strength Tablet, Chewable
NDC Package 21130-310-72
Package Information
Ultra Strength (calcium carbonate) tablets is a medication used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. This formulation utilizes a tablet, chewable delivery system. Marketed by Better Living Brands Llc, this product is identified by NDC 21130-310 and is authorized under FDA application M001.
Identification & Billing
- RxCUI: 308892 - calcium carbonate 1000 MG (Ca 400 MG) Chewable Tablet
- RxCUI: 308892 - calcium carbonate 1000 MG Chewable Tablet
- RxCUI: 308892 - calcium carbonate 1000 MG (calcium 400 MG) Chewable Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 21130 - Better Living Brands Llc
- 21130-310 - Ultra Strength
- 21130-310-72 - 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
- 21130-310 - Ultra Strength
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (21130-310). Click a package code to view its specific billing and regulatory data.
* 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 21130-310-72 identifies a specific commercial package of 72 tablet, chewable in 1 bottle, plastic of Ultra Strength, a human over the counter drug labeled by Better Living Brands Llc. This tablet, chewable is formulated for oral use and contains calcium carbonate 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 Better Living Brands Llc on September 30, 2020. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
This medication is used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. It is an antacid that works by lowering the amount of acid in the stomach. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
How is this Better Living Brands Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 21130031072. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.