Walgreens Antacid Pain Relief Extra Strength Tablet, Effervescent
NDC Package 0363-0541-36

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Walgreens Antacid Pain Relief Extra Strength (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 Walgreens, this product is identified by NDC 0363-0541 and is authorized under FDA application M013.

Identification & Billing

NDC Package Code
0363-0541-36
Package Description
18 POUCH in 1 CARTON / 2 TABLET, EFFERVESCENT in 1 POUCH
Product Code
0363-0541
11-Digit Billing Format
00363054136
RxNorm Crosswalk
  • RxCUI: 1536833 - aspirin 500 MG / citric acid 1000 MG / sodium bicarbonate 1985 MG Effervescent Oral Tablet
  • RxCUI: 1536833 - ASA 500 MG / Citric Acid 1000 MG / NaHCO3 1985 MG Effervescent Oral Tablet

Clinical Specifications

Proprietary Name
Walgreens Antacid Pain Relief Extra Strength
Non-Proprietary Name
Aspirin, Citric Acid, Sodium Bicarbonate
Substance Name
Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate
Dosage Form
Tablet, Effervescent - A solid dosage form containing mixtures of acids (e.g., citric acid, tartaric acid) and sodium bicarbonate, which release carbon dioxide when dissolved in water; it is intended to be dissolved or dispersed in water before administration.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
■ do not exceed recommended dosage■ to avoid serious injury, completely dissolve tablets in 4 oz. of water before takingadults and children 12 years and over (up to 60 years of age): 2 tablets every 4 hours do not exceed 8 tablets in 24 hours60 years and over: 2 tablets every 4 hours do not exceed 4 tablets in 24 hoursChildren under 12 years: consult a doctor

Regulatory & Marketing

Labeler Name
Walgreens
Product Type
Human Otc Drug
FDA Application #
M013
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-05-2021
End Marketing Date
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0363-0541-36 identifies a specific commercial package of 18 pouch in 1 carton / 2 tablet, effervescent in 1 pouch of Walgreens Antacid Pain Relief Extra Strength, a human over the counter drug labeled by Walgreens. 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 Walgreens on February 05, 2021.

How is this Walgreens product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363054136. 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:

10-Digit Format (4-4-2)
0363-0541-36
11-Digit CMS (5-4-2)
00363-0541-36

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.