NDC 70449-1001 Allergy Bee Gone

Kali Bichromicum 6x,Sabadilla 6x,Luffa Operculata 6x Liquid Nasal - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
70449-1001
Proprietary Name:
Allergy Bee Gone
Non-Proprietary Name: [1]
Kali Bichromicum 6x, Sabadilla 6x, Luffa Operculata 6x
Substance Name: [2]
Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Luffa Operculata Fruit; Potassium Dichromate; Schoenocaulon Officinale Seed
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Nasal - Administration to the nose; administered by way of the nose.
  • Labeler Name: [5]
    Buzzagogo, Inc
    Labeler Code:
    70449
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-09-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    BROWN (C48332)

    Product Packages

    NDC Code 70449-1001-1

    Package Description: 1 TUBE in 1 BOX / 10 mL in 1 TUBE

    Product Details

    What is NDC 70449-1001?

    The NDC code 70449-1001 is assigned by the FDA to the product Allergy Bee Gone which is a human over the counter drug product labeled by Buzzagogo, Inc. The generic name of Allergy Bee Gone is kali bichromicum 6x, sabadilla 6x, luffa operculata 6x. The product's dosage form is liquid and is administered via nasal form. The product is distributed in a single package with assigned NDC code 70449-1001-1 1 tube in 1 box / 10 ml in 1 tube. 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 Allergy Bee Gone 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 Allergy Bee Gone UNII Codes?

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

    • POTASSIUM DICHROMATE (UNII: T4423S18FM)
    • DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
    • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
    • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
    • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
    • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
    • GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E)
    • GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (Active Moiety)
    • HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
    • HISTAMINE (UNII: 820484N8I3) (Active Moiety)

    Which are Allergy Bee Gone 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".