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  4. NDC Product Code: 72363-028 Nozin Allergy Master

NDC 72363-028 Nozin Allergy Master

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72363-028?
  4. Nozin Allergy Master 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) 72363-028 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:
72363-028
Proprietary Name:
Nozin Allergy Master
Product Type: [3]
Labeler Name: [5]
Ag Essence
Labeler Code:
72363
Product Label ID:
11c0c002-0746-79fa-e063-6394a90aff28
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
03-04-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
U
Code Navigator:

Code Structure Chart

Product Details

What is NDC 72363-028?

The NDC code 72363-028 is assigned by the FDA to the product Nozin Allergy Master which is product labeled by Ag Essence. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72363-028-03 1 bottle, spray in 1 box / 10 g in 1 bottle, spray. 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 Nozin Allergy Master?

Adults and childrenover 12 years of age (Also see illustrations on right side)remove cap and safety cliphold with thumb at bottomof bottles and nozzle between your fingerson first use, prime the pump by depressing several timesplace nozzle tip to just inside nasal openingpimp once into each nostrilwipe away nasal drainagemay use up to 3 times per daychildren under 12 years of age shgould be supervisedchildren under 2 years of age ask a doctor before use

Which are Nozin Allergy Master UNII Codes?

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

  • GALPHIMIA GLAUCA WHOLE (UNII: RW4TS05W0D)
  • GALPHIMIA GLAUCA WHOLE (UNII: RW4TS05W0D) (Active Moiety)
  • CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
  • CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) (Active Moiety)

Which are Nozin Allergy Master 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.

[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".