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NDC 72363-028 Nozin Allergy Master

Galphimia Glauca,Citrus Vulgaris Spray Topical - 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
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
72363-028
Proprietary Name:
Nozin Allergy Master
Non-Proprietary Name: [1]
Galphimia Glauca, Citrus Vulgaris
Substance Name: [2]
Citrus Aurantium Fruit Oil; Galphimia Glauca Whole
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • 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]
    N
    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 a human over the counter drug product labeled by Ag Essence. The generic name of Nozin Allergy Master is galphimia glauca, citrus vulgaris. The product's dosage form is spray and is administered via topical form. 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

    What are Nozin Allergy Master Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    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:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [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 ("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".