Heb Stomach Relief
NDC Package 37808-152-06

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Heb Stomach Relief is shake well before usemL = milliliterTBSP = tablespoonadults and children 12 years and over: 1 dose (2 TBSP or 30 mL) every 1/2 to 1 hour as neededdo not exceed 8 doses (16 TBSP or 240 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. Marketed by H E B, this product is identified by NDC 37808-152 and is authorized under FDA application M008.

Identification & Billing

NDC Package Code
37808-152-06
Package Description
473 mL in 1 BOTTLE
Product Code
37808-152
11-Digit Billing Format
37808015206
RxNorm Crosswalk
  • RxCUI: 308762 - bismuth subsalicylate 525 MG in 30 mL Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 17.5 MG/ML Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 1.75 % Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 262 MG per 15 ML Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 524 MG per 30 ML Oral Suspension

Clinical Specifications

Proprietary Name
Heb Stomach Relief
Dosage Form
-
Usage Information
Shake well before usemL = milliliterTBSP = tablespoonadults and children 12 years and over: 1 dose (2 TBSP or 30 mL) every 1/2 to 1 hour as neededdo not exceed 8 doses (16 TBSP or 240 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

Regulatory & Marketing

Labeler Name
H E B
FDA Application #
M008
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-28-2018
Listing Expiration
12-31-2025
Exclude Flag
I
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (37808-152). Click a package code to view its specific billing and regulatory data.

37808-152-04
237 mL in 1 BOTTLE

* 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 37808-152-06 identifies a specific commercial package of 473 ml in 1 bottle of Heb Stomach Relief, labeled by H E B. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by H E B on September 28, 2018. The current certification is valid through December 31, 2025.

How is this H E B product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808015206. 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 (5-3-2)
37808-152-06
11-Digit CMS (5-4-2)
37808-0152-06

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