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  4. NDC Product Code: 75981-007 Goodsense Medicated Pads

NDC 75981-007 Goodsense Medicated Pads

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75981-007?
  4. Goodsense Medicated Pads 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:
75981-007
Proprietary Name:
Goodsense Medicated Pads
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Geiss, Destin And Dunn, Inc.
Labeler Code:
75981
Product Label ID:
afa3ed3f-42e9-4839-8bb8-a5c2b4c9b1f1
Start Marketing Date: [9]
06-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 75981-007?

The NDC code 75981-007 is assigned by the FDA to the product Goodsense Medicated Pads which is product labeled by Geiss, Destin And Dunn, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75981-007-47 100 applicator in 1 jar / 2.5 ml in 1 applicator. 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 Goodsense Medicated Pads?

DirectionsAs hemorrhoidal treatment for adults:When practical clean the affected area with mild soap and warm water and rinse thoroughlyGently dry by patting or blotting with toilet tissue or soft cloth before applyingGently apply to the affected area by patting and then discardCan be used up to six times daily or after each bowel movementChildren under 12 years of age: ask a doctor

Which are Goodsense Medicated Pads UNII Codes?

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

Which are Goodsense Medicated Pads 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 Goodsense Medicated Pads?

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".