Relief Otc Antacid
NDC Package 69016-001-18
Package Information
Relief Otc Antacid is do not use if outer seal is broken, replace cap tightlyDo not exceed daily recommended dosageShake well & drink 2-4 ounces as symptoms occur Adults and children 12 years and over Up to 4oz. Marketed by Tummy Company, Inc., this product is identified by NDC 69016-001 and is authorized under FDA application part331.
Identification & Billing
- RxCUI: 1538288 - calcium 545 MG / potassium 905 MG / sodium bicaronate 2110 MG in 118 mL Oral Suspension
- RxCUI: 1538288 - calcium carbonate 4.62 MG/ML / potassium bicarbonate 7.67 MG/ML / sodium bicarbonate 17.9 MG/ML Oral Suspension
- RxCUI: 1538288 - calcium 545 MG / potassium 905 MG / sodium bicaronate 2110 MG per 118 ML Oral Suspension
- RxCUI: 1538288 - Calcium Carbonate 4.62 MG/ML / K+ bicarbonate 7.67 MG/ML / NaHCO3 17.9 MG/ML Oral Suspension
- RxCUI: 1538288 - Calcium Carbonate 4.62 MG/ML / Pot bicarbonate 7.67 MG/ML / NaHCO3 17.9 MG/ML Oral Suspension
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69016 - Tummy Company, Inc.
- 69016-001 - Relief Otc Antacid
- 69016-001-18 - 118 mL in 1 BOTTLE
- 69016-001 - Relief Otc Antacid
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 (69016-001). 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 69016-001-18 identifies a specific commercial package of 118 ml in 1 bottle of Relief Otc Antacid, labeled by Tummy Company, 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 Tummy Company, Inc. on May 28, 2014. The current certification is valid through December 31, 2017.
How is this Tummy Company, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69016000118. 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.