1. Home
  2. Labeler Index
  3. Similasan Corporation
  4. NDC Product Code: 59262-245 Kids Nasal Allergy Relief

NDC 59262-245 Kids Nasal Allergy Relief

Cardiospermum Halicacabum Flowering Top,Galphimia Glauca Flowering Top,Luffa Operculata - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59262-245?
  4. Kids Nasal Allergy Relief Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
59262-245
Proprietary Name:
Kids Nasal Allergy Relief
Non-Proprietary Name: [1]
Cardiospermum Halicacabum Flowering Top, Galphimia Glauca Flowering Top, Luffa Operculata Fruit And Schoenocaulon Officinale Seed
Substance Name: [2]
Cardiospermum Halicacabum Flowering Top; Galphimia Glauca Flowering Top; Luffa Operculata Fruit; Schoenocaulon Officinale Seed
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]
  • Nasal - Administration to the nose; administered by way of the nose.
    • Labeler Name: [5]
    Similasan Corporation
    Labeler Code:
    59262
    Product Label ID:
    627be5fc-5a19-48c5-939a-f0b5b2625531
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-15-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 59262-245-20

    Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 20 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 59262-245?

    The NDC code 59262-245 is assigned by the FDA to the product Kids Nasal Allergy Relief which is a human over the counter drug product labeled by Similasan Corporation. The generic name of Kids Nasal Allergy Relief is cardiospermum halicacabum flowering top, galphimia glauca flowering top, luffa operculata fruit and schoenocaulon officinale seed. The product's dosage form is spray and is administered via nasal form. The product is distributed in a single package with assigned NDC code 59262-245-20 1 bottle, spray in 1 carton / 20 ml 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 Kids Nasal Allergy Relief?

    For adults and children ages 2 and over:• Remove tamper-evident plastic seal from bottle• Lift cap off bottle• Spray 1-3 times into each nostril• Use as needed• Replace cap after use

    What are Kids Nasal Allergy Relief 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 Kids Nasal Allergy Relief UNII Codes?

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

    • CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)
    • CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR) (Active Moiety)
    • GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E)
    • GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (Active Moiety)
    • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
    • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
    • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
    • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)

    Which are Kids Nasal Allergy Relief 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".