Alka-seltzer Kids Tummy Reliefchews Tablet, Chewable
NDC Package 0280-0051-01
Package Information
Alka-seltzer Kids Tummy Reliefchews (calcium carbonate and dimethicone) tablets is uses for the relief of: ● acid indigestion ● heartburn ● sour stomach ● upset stomach associated with these symptoms ● bloating, pressure, or stuffed feeling commonly referred to as gas. This formulation utilizes a tablet, chewable delivery system. Marketed by Bayer Healthcare Llc., this product is identified by NDC 0280-0051 and is authorized under FDA application M001.
Identification & Billing
Clinical Specifications
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Skin Barrier Activity - [PE] (Physiologic Effect)
Regulatory & Marketing
Hierarchy Structure
- 0280 - Bayer Healthcare Llc.
- 0280-0051 - Alka-seltzer Kids Tummy Reliefchews
- 0280-0051-01 - 28 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
- 0280-0051 - Alka-seltzer Kids Tummy Reliefchews
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0280-0051-01 identifies a specific commercial package of 28 tablet, chewable in 1 bottle, plastic of Alka-seltzer Kids Tummy Reliefchews, a human over the counter drug labeled by Bayer Healthcare Llc.. This tablet, chewable is formulated for oral use and contains calcium carbonate; dimethicone 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 Bayer Healthcare Llc. on March 01, 2021. The current certification is valid through December 31, 2026.
How is this Bayer Healthcare Llc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00280005101. 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 Labeler segment to maintain the 5-4-2 structure.