Hemorrhoidal Starch
NDC Package 50730-1512-1

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.

Hemorrhoidal Starch is adults:When practical, cleanse the affected area with mild soap and warm water. Marketed by H And P Industries, Inc. Dba Triad Group, this product is identified by NDC 50730-1512 and is authorized under FDA application part346.

Identification & Billing

NDC Package Code
50730-1512-1
Package Description
12 SUPPOSITORY in 1 BOX
Product Code
50730-1512
11-Digit Billing Format
50730151201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hemorrhoidal Starch
Dosage Form
-
Usage Information
Adults:When practical, cleanse the affected area with mild soap and warm water. Rinse thoroughly.Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product.Detach one suppository from strip of suppositories.Remove film before inserting into the rectum by holding the suppository upright. Carefully separate film by inserting tip of fingernail at film split.Carefully peel film slowly and evenly down both sides to expose suppositoryAvoid excessive handling of suppository, which is designed to melt at body temperature. If suppository seems soft, hold in film wrapper under cold water for 2 or 3 minutes.Insert one suppository rectally up to 6 times daily or after each bowel movementChildren under 12 years: ask a doctor.

Regulatory & Marketing

Labeler Name
H And P Industries, Inc. Dba Triad Group
FDA Application #
part346
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-01-2006
Listing Expiration
12-31-2017
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 50730-1512-1 identifies a specific commercial package of 12 suppository in 1 box of Hemorrhoidal Starch, labeled by H And P Industries, Inc. Dba Triad Group. 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 And P Industries, Inc. Dba Triad Group on August 01, 2006. The current certification is valid through December 31, 2017.

How is this H And P Industries, Inc. Dba Triad Group product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50730151201. 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 (5-4-1)
50730-1512-1
11-Digit CMS (5-4-2)
50730-1512-01

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