Quality Choice Stomach Relief 528 Liquid
NDC Package 83324-021-08
Package Information
Quality Choice Stomach Relief 528 (bismuth subsalicylate) liquids is shake well before usemL = milliliterTBSP = tablespoonadults and children 12 years and over: 1 dose (2 TBSP or 15 mL) every 1/2 hour as neededdo not exceed 8 doses (120 mL) in 24 hoursuse until diarrhea stops but not more than 2 dayschildren under 12 years: ask a doctordrink plenty of fluids to help prevent dehydration caused by diarrhea. This formulation utilizes a liquid delivery system. Marketed by Chain Drug Marketing Association Inc., this product is identified by NDC 83324-021 and is authorized under FDA application M008.
Identification & Billing
- RxCUI: 308763 - bismuth subsalicylate 1050 MG in 30 mL Oral Suspension
- RxCUI: 308763 - bismuth subsalicylate 35 MG/ML Oral Suspension
- RxCUI: 308763 - bismuth subsalicylate 1050 MG per 30 ML Oral Suspension
- RxCUI: 308763 - bismuth subsalicylate 525 MG per 15 ML Oral Suspension
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 83324 - Chain Drug Marketing Association Inc.
- 83324-021 - Quality Choice Stomach Relief 528
- 83324-021-08 - 236 mL in 1 BOTTLE
- 83324-021 - Quality Choice Stomach Relief 528
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 83324-021-08 identifies a specific commercial package of 236 ml in 1 bottle of Quality Choice Stomach Relief 528, a human over the counter drug labeled by Chain Drug Marketing Association Inc.. This liquid is formulated for oral use and contains bismuth subsalicylate 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 Chain Drug Marketing Association Inc. on April 19, 2024. The current certification is valid through December 31, 2026.
How is this Chain Drug Marketing Association Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 83324002108. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 236 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.