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  4. NDC Product Code: 49781-077 Leader Hemorrholidal

NDC 49781-077 Leader Hemorrholidal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49781-077?
  4. Leader Hemorrholidal 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:
49781-077
Proprietary Name:
Leader Hemorrholidal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
49781
Product Label ID:
f5bd4007-75f8-40ef-ba32-8eba475847e1
Start Marketing Date: [9]
12-10-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49781-077-02

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

Product Details

What is NDC 49781-077?

The NDC code 49781-077 is assigned by the FDA to the product Leader Hemorrholidal which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49781-077-02 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 Leader Hemorrholidal?

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 Leader Hemorrholidal UNII Codes?

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

Which are Leader Hemorrholidal 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 Leader Hemorrholidal?

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:
  • RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine HCl 0.25 % Rectal Ointment
  • RxCUI: 1372298 - mineral oil 0.14 MG/MG / petrolatum 0.749 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Ointment
  • RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine hydrochloride 0.25 % Rectal Ointment

* Please review the disclaimer below.

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".