Publix Fast Relief Effervescent Tablet, Effervescent
NDC Package 56062-421-68
Package Information
Publix Fast Relief Effervescent (aspirin, citric acid, sodium bicarbonate) tablets is ■ do not exceed recommended dosage■ to avoid serious injury, completely dissolve tablets in 4 oz. This formulation utilizes a tablet, effervescent delivery system. Marketed by Publix Super Markets Inc., this product is identified by NDC 56062-421 and is authorized under FDA application M013.
Identification & Billing
- RxCUI: 1536675 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet
- RxCUI: 1536675 - ASA 325 MG / Citric Acid 1000 MG / NaHCO3 1916 MG Effervescent Oral Tablet
Clinical Specifications
- Acidifying Activity - [MoA] (Mechanism of Action)
- Alkalinizing Activity - [MoA] (Mechanism of Action)
- Anti-Inflammatory Agents, Non-Steroidal - [CS]
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
- Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Decreased Platelet Aggregation - [PE] (Physiologic Effect)
- Decreased Prostaglandin Production - [PE] (Physiologic Effect)
- Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
- Platelet Aggregation Inhibitor - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 56062 - Publix Super Markets Inc.
- 56062-421 - Publix Fast Relief Effervescent
- 56062-421-68 - 18 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
- 56062-421 - Publix Fast Relief Effervescent
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 56062-421-68 identifies a specific commercial package of 18 pouch in 1 carton / 2 tablet, effervescent in 1 pouch of Publix Fast Relief Effervescent, a human over the counter drug labeled by Publix Super Markets Inc.. This product is billed for "EA" each discreet unit and contains an estimated amount of 18 billable units per package. This tablet, effervescent is formulated for oral use and contains anhydrous citric acid; aspirin; sodium bicarbonate 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 Publix Super Markets Inc. on November 10, 2011.
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: 56062042168. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 18 total billable units per package. 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.