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  4. NDC Product Code: 65923-778 Shopko Hemorrhoidal

NDC 65923-778 Shopko Hemorrhoidal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65923-778?
  4. Shopko Hemorrhoidal Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
65923-778
Proprietary Name:
Shopko Hemorrhoidal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Exchange Corp
Labeler Code:
65923
Product Label ID:
01f99bcc-171d-466e-a636-40ed294e9b72
Start Marketing Date: [9]
06-30-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 65923-778-57

Package Description: 1 TUBE in 1 CARTON / 57 g in 1 TUBE

Product Details

What is NDC 65923-778?

The NDC code 65923-778 is assigned by the FDA to the product Shopko Hemorrhoidal which is product labeled by United Exchange Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65923-778-57 1 tube in 1 carton / 57 g in 1 tube. 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 Shopko Hemorrhoidal?

Directionschildren under 12 years of age: ask a doctoradults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipegently dry by patting or blotting with a tissue or a soft cloth before applyingwhen first opening tube, remove foil sealfor intrarectal use: remove protective cover from applicator and attach to tubelubricate applicator well, then gently insert applicator into the rectumthoroughly clean applicator and replace protective cover after each useapply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movementalso apply ointment to external area

Which are Shopko Hemorrhoidal UNII Codes?

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

Which are Shopko Hemorrhoidal 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:

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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".