Heb Maximum Strength Pain Relief Hemorrhoidal
NDC Package 37808-992-24

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 Maximum Strength Pain Relief Hemorrhoidal is adults:when practical, cleanse affected area by patting or blotting with appropriate cleansing wipe. Marketed by Heb, this product is identified by NDC 37808-992 and is authorized under FDA application part346.

Identification & Billing

NDC Package Code
37808-992-24
Package Description
1 TUBE in 1 CARTON / 56.7 g in 1 TUBE
Product Code
37808-992
11-Digit Billing Format
37808099224

Clinical Specifications

Proprietary Name
Heb Maximum Strength Pain Relief Hemorrhoidal
Dosage Form
-
Usage Information
Adults:when practical, cleanse affected area by patting or blotting with appropriate cleansing wipe. Gently dry by patting or blotting with tissue or soft cloth before applying cream.when first opening tube, remove foil sealapply externally or in lower portion of anal canal onlyapply externally to affected area up to 4 times daily, especially at night, in the morning, or after each bowel movementfor application in lower anal canal; remove cover from dispensing cap. Attach dispensing cap to tube. Lubriate dispensing cap well, then gently insert dispensing cap partway into anus thoroughly cleanse dispensing cap after each use, and replace coverChildren under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Heb
FDA Application #
part346
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
10-18-2018
Listing Expiration
12-31-2024
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 37808-992-24 identifies a specific commercial package of 1 tube in 1 carton / 56.7 g in 1 tube of Heb Maximum Strength Pain Relief Hemorrhoidal, 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 October 18, 2018. The current certification is valid through December 31, 2024.

How is this Heb product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37808099224. 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)
37808-992-24
11-Digit CMS (5-4-2)
37808-0992-24

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