Allergena For Pets
NDC 62713-943

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 62713-943?
  4. Allergena For Pets 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.

Allergena For Pets is a UNAPPROVED HOMEOPATHIC-approved product labeled by Meditrend, Inc. Dba Progena Professional Formulations. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 62713-943 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
62713-943
Proprietary Name:
Allergena For Pets
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Meditrend, Inc. Dba Progena Professional Formulations
Labeler Code:
62713
Product Label ID:
42d26711-4fde-4835-80b1-0a72cc1570d7
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-01-1987
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 62713-943?

The NDC code 62713-943 is assigned by the FDA to the product Allergena For Pets. This pharmaceutical product is labeled by Meditrend, Inc. Dba Progena Professional Formulations and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 62713-943-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Use:  This product is a Homeopathic Dilution formulated to improve immunity for the temporary relief of allergies.

Which are the associated UNII Codes?

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

  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
  • BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY)
  • BETULA PAPYRIFERA POLLEN (UNII: 3538FNV8AY) (Active Moiety)
  • JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y)
  • JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (Active Moiety)
  • QUERCUS RUBRA POLLEN (UNII: SVW19ET93C)
  • QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (Active Moiety)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
  • SALSOLA TRAGUS POLLEN (UNII: V174354MDI)
  • SALSOLA TRAGUS POLLEN (UNII: V174354MDI) (Active Moiety)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
  • POA ANNUA POLLEN (UNII: 7U437HHU5C)
  • POA ANNUA POLLEN (UNII: 7U437HHU5C) (Active Moiety)
  • LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0)
  • LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0) (Active Moiety)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
  • DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K)
  • DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K) (Active Moiety)
  • DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q)
  • DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q) (Active Moiety)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • MYRRH (UNII: JC71GJ1F3L)
  • MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
  • NASTURTIUM OFFICINALE (UNII: YH89GMV676)
  • NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • FENUGREEK LEAF (UNII: 487RI96K8Z)
  • FENUGREEK LEAF (UNII: 487RI96K8Z) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
  • DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
  • URTICA URENS (UNII: IHN2NQ5OF9)
  • URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".