Equaline Effervescent Antacid And Pain Relief Tablet, Effervescent
NDC Package 41163-421-68
Package Information
Equaline Effervescent Antacid And Pain Relief (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 United Natural Foods, Inc. Dba Unfi, this product is identified by NDC 41163-421 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
- 41163 - United Natural Foods, Inc. Dba Unfi
- 41163-421 - Equaline Effervescent Antacid And Pain Relief
- 41163-421-68 - 18 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
- 41163-421 - Equaline Effervescent Antacid And Pain Relief
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 41163-421-68 identifies a specific commercial package of 18 pouch in 1 carton / 2 tablet, effervescent in 1 pouch of Equaline Effervescent Antacid And Pain Relief, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. 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 United Natural Foods, Inc. Dba Unfi on November 16, 2014.
How is this United Natural Foods, Inc. Dba Unfi product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 41163042168. 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.