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  4. NDC Product Code: 50730-1512 Hemorrhoidal Starch

NDC 50730-1512 Hemorrhoidal Starch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50730-1512?
  4. Hemorrhoidal Starch Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50730-1512
Proprietary Name:
Hemorrhoidal Starch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H And P Industries, Inc. Dba Triad Group
Labeler Code:
50730
Product Label ID:
6a3ee178-39a9-44bf-8fdb-5eacbd089998
Start Marketing Date: [9]
08-01-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 50730-1512?

The NDC code 50730-1512 is assigned by the FDA to the product Hemorrhoidal Starch which is product labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50730-1512-1 12 suppository in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Hemorrhoidal Starch?

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.

Which are Hemorrhoidal Starch UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Hemorrhoidal Starch Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Hemorrhoidal Starch?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".