Heb Diarrhea Relief
NDC Package 37808-173-12

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

Package Information

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

Heb Diarrhea Relief is •shake well immediately before each use•adults and children 12 years of age and older: 30 ml or 2 tablespoonful•for accurate dosing, use convenient pre-measured dose cup•repeat dose every 1/2 hour to 1 hour as needed•do not exceed 8 doses in 24 hours•use until diarrhea stops but not more than 2 days•children under 12 years: ask a doctor•drink plenty of clear fluids to help prevent dehydration caused by diarrhea. Marketed by Heb, this product is identified by NDC 37808-173 and is authorized under FDA application part335.

Identification & Billing

NDC Package Code
37808-173-12
Package Description
355 mL in 1 BOTTLE, PLASTIC
Product Code
37808-173
11-Digit Billing Format
37808017312
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 Diarrhea Relief Vanilla Flavor
Dosage Form
-
Usage Information
•shake well immediately before each use•adults and children 12 years of age and older: 30 ml or 2 tablespoonful•for accurate dosing, use convenient pre-measured dose cup•repeat dose every 1/2 hour to 1 hour as needed•do not exceed 8 doses in 24 hours•use until diarrhea stops but not more than 2 days•children under 12 years: ask a doctor•drink plenty of clear fluids to help prevent dehydration caused by diarrhea

Regulatory & Marketing

Labeler Name
Heb
FDA Application #
part335
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
05-14-2019
Listing Expiration
12-31-2023
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 37808-173-12 identifies a specific commercial package of 355 ml in 1 bottle, plastic of Heb Diarrhea Relief Vanilla Flavor, labeled by Heb. 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 Heb on May 14, 2019. The current certification is valid through December 31, 2023.

How is this Heb product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808017312. 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)
37808-173-12
11-Digit CMS (5-4-2)
37808-0173-12

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