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  4. NDC Product Code: 50114-6134 Abropernol

NDC 50114-6134 Abropernol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50114-6134?
  5. Abropernol Uses
  6. Active Ingredients UNII Codes
  7. 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:
50114-6134
Proprietary Name:
Abropernol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heel Inc
Labeler Code:
50114
Product Label ID:
adfe12ec-eea8-43a2-a283-45b1f63204a8
Start Marketing Date: [9]
01-31-1984
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
HEEL
Score:
1

Code Structure Chart

Product Details

What is NDC 50114-6134?

The NDC code 50114-6134 is assigned by the FDA to the product Abropernol 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 50114-6134-2 30000 mg in 1 bottle . 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 Abropernol?

For the temporary relief of:DermatitusMinor skin irritationsEczema, hyperhidrosisHyperkeratosis

Which are Abropernol UNII Codes?

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

  • ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
  • ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
  • CALCIUM FLUORIDE (UNII: O3B55K4YKI)
  • CALCIUM FLUORIDE (UNII: O3B55K4YKI) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
  • AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037)
  • AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
  • NITRIC ACID (UNII: 411VRN1TV4)
  • NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
  • KEROSENE (UNII: 1C89KKC04E)
  • KEROSENE (UNII: 1C89KKC04E) (Active Moiety)

Which are Abropernol 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:

* 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".