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  4. NDC Product Code: 48951-3117 Conchae Argentum

NDC 48951-3117 Conchae Argentum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 48951-3117?
  4. Conchae Argentum 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 expired due to lack of listing certification.

Get all the details for National Drug Code (NDC) 48951-3117 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
48951-3117
Proprietary Name:
Conchae Argentum
Product Type: [3]
Labeler Name: [5]
Uriel Pharmacy Inc.
Labeler Code:
48951
Product Label ID:
29907010-b436-434b-951f-04fbcb00e955
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
09-01-2009
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
U
Code Navigator:

Code Structure Chart

Product Details

What is NDC 48951-3117?

The NDC code 48951-3117 is assigned by the FDA to the product Conchae Argentum which is product labeled by Uriel Pharmacy Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 48951-3117-1 10 ampule in 1 box / 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 Conchae Argentum?

Directions: FOR ORAL USE.

Which are Conchae Argentum UNII Codes?

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

  • DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X)
  • DRYOPTERIS FILIX-MAS ROOT (UNII: C0ZK0RRF5X) (Active Moiety)
  • PTERIDIUM AQUILINUM WHOLE (UNII: 05T3M06HCM)
  • PTERIDIUM AQUILINUM WHOLE (UNII: 05T3M06HCM) (Active Moiety)
  • ASPLENIUM SCOLOPENDRIUM WHOLE (UNII: L3ZLR659ZI)
  • ASPLENIUM SCOLOPENDRIUM WHOLE (UNII: L3ZLR659ZI) (Active Moiety)
  • SILVER (UNII: 3M4G523W1G)
  • SILVER (UNII: 3M4G523W1G) (Active Moiety)
  • OSTREA EDULIS SHELL (UNII: 49OY13BE7Z)
  • OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (Active Moiety)
  • AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
  • AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)

Which are Conchae Argentum 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".