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  4. NDC Product Code: 50114-5324 Psorinoheel

NDC 50114-5324 Psorinoheel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50114-5324?
  4. Psorinoheel 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:
50114-5324
Proprietary Name:
Psorinoheel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heel Inc
Labeler Code:
50114
Product Label ID:
5c31cacd-c3e1-4241-beca-29f1b28a6fd1
Start Marketing Date: [9]
01-31-1993
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50114-5324?

The NDC code 50114-5324 is assigned by the FDA to the product Psorinoheel which is product labeled by Heel Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50114-5324-6 10 ampule in 1 carton / 1.1 ml in 1 ampule. 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 Psorinoheel?

ContraindicationsPsorinoheel® Oral Vials are contraindicated in patients with known hypersensitivity to Psorinoheel® or any of its ingredients.

Which are Psorinoheel UNII Codes?

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

  • SULFUR (UNII: 70FD1KFU70)
  • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK)
  • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (Active Moiety)
  • BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q)
  • BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (Active Moiety)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (Active Moiety)
  • GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F)
  • GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (Active Moiety)
  • NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
  • NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (Active Moiety)
  • CICUTA VIROSA ROOT (UNII: YEA9P21S8N)
  • CICUTA VIROSA ROOT (UNII: YEA9P21S8N) (Active Moiety)
  • POTASSIUM DICHROMATE (UNII: T4423S18FM)
  • DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)

Which are Psorinoheel 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".