NDC 44911-0674 Histastat Pollen

Baptisia Tinctoria,Echinacea (angustifolia),Adrenalinum,Allium Cepa,Ambrosia - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
44911-0674
Proprietary Name:
Histastat Pollen
Non-Proprietary Name: [1]
Baptisia Tinctoria, Echinacea (angustifolia), Adrenalinum, Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Euphrasia Officinalis, Histaminum Hydrochloricum, Natrum Muriaticum, Natrum Sulphuricum, Nux Vomica, Phosphorus, Pulsatilla (pratensis), Sabadilla, Sinapis Nigra, Solidago Virgaurea, Sulphur, Wyethia Helenioides
Substance Name: [2]
Ambrosia Artemisiifolia Whole; Arsenic Trioxide; Baptisia Tinctoria Root; Black Mustard Seed; Echinacea Angustifolia Whole; Epinephrine; Euphrasia Stricta; Histamine Dihydrochloride; Onion; Phosphorus; Pulsatilla Pratensis Whole; Schoenocaulon Officinale Seed; Sodium Chloride; Sodium Sulfate; Solidago Virgaurea Flowering Top; Strychnos Nux-vomica Seed; Sulfur; Wyethia Helenioides Root
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]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Labeler Code:
    44911
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-12-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 44911-0674?

    The NDC code 44911-0674 is assigned by the FDA to the product Histastat Pollen which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Histastat Pollen is baptisia tinctoria, echinacea (angustifolia), adrenalinum, allium cepa, ambrosia artemisiaefolia, arsenicum album, euphrasia officinalis, histaminum hydrochloricum, natrum muriaticum, natrum sulphuricum, nux vomica, phosphorus, pulsatilla (pratensis), sabadilla, sinapis nigra, solidago virgaurea, sulphur, wyethia helenioides. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 44911-0674-1 30 ml in 1 bottle, dropper . 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 Histastat Pollen?

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

    What are Histastat Pollen 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 Histastat Pollen UNII Codes?

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

    Which are Histastat Pollen 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:

    Which are the Pharmacologic Classes for Histastat Pollen?

    * 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".