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  4. NDC Product Code: 43406-0106 Allergy New England Mix

NDC 43406-0106 Allergy New England Mix

Betula Pubescens Bark,Artemisia Vulgaris Pollen,Plantago Lanceolata Pollen,Acer - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43406-0106?
  4. Allergy New England Mix Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43406-0106
Proprietary Name:
Allergy New England Mix
Non-Proprietary Name: [1]
Betula Pubescens Bark, Artemisia Vulgaris Pollen, Plantago Lanceolata Pollen, Acer Pseudoplatanus Pollen, Betula Pubescens Bark, Evernia Prunastri Bark, Armaranthus Retroflexus Pollen, Pinus Massoniana Pollen, Tabuliformis Pollen, Ambrosia Artemisifolia Pollen,
Substance Name: [2]
Acer Pseudoplatanus Pollen; Amaranthus Retroflexus Pollen; Ambrosia Artemisiifolia Pollen; Artemisia Vulgaris Pollen; Betula Pubescens Bark; Evernia Prunastri; Juniperus Virginiana Pollen; Morus Rubra Pollen; Pinus Massoniana Pollen; Pinus Tabuliformis Pollen; Plantago Lanceolata Pollen; Populus Alba Pollen; Rumex Acetosella Pollen
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]
    Natural Creations, Inc.
    Labeler Code:
    43406
    Product Label ID:
    b12b20c3-a7bf-4366-89da-a8023204048e
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-29-2007
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43406-0106?

    The NDC code 43406-0106 is assigned by the FDA to the product Allergy New England Mix which is a human over the counter drug product labeled by Natural Creations, Inc.. The generic name of Allergy New England Mix is betula pubescens bark, artemisia vulgaris pollen, plantago lanceolata pollen, acer pseudoplatanus pollen, betula pubescens bark, evernia prunastri bark, armaranthus retroflexus pollen, pinus massoniana pollen, tabuliformis pollen, ambrosia artemisifolia pollen, . 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 43406-0106-1 30 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 Allergy New England Mix?

    Uses:  Temporarily relieves sneezing, watery-itchy eyes, coughing, nasal congestion, runny nose &/or other symptoms related to outdoor allergies.**

    What are Allergy New England Mix 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 New England Mix UNII Codes?

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

    • BETULA PUBESCENS BARK (UNII: 3R504894L9)
    • BETULA PUBESCENS BARK (UNII: 3R504894L9) (Active Moiety)
    • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
    • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
    • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
    • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
    • ACER PSEUDOPLATANUS POLLEN (UNII: W8RT4P7T0H)
    • ACER PSEUDOPLATANUS POLLEN (UNII: W8RT4P7T0H) (Active Moiety)
    • EVERNIA PRUNASTRI (UNII: O3034Q5AHK)
    • EVERNIA PRUNASTRI (UNII: O3034Q5AHK) (Active Moiety)
    • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
    • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
    • PINUS MASSONIANA POLLEN (UNII: D209654E9Q)
    • PINUS MASSONIANA POLLEN (UNII: D209654E9Q) (Active Moiety)
    • PINUS TABULIFORMIS POLLEN (UNII: 60EUO12HBX)
    • PINUS TABULIFORMIS POLLEN (UNII: 60EUO12HBX) (Active Moiety)
    • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
    • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
    • JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G)
    • JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (Active Moiety)
    • MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52)
    • MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (Active Moiety)
    • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW)
    • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (Active Moiety)
    • POPULUS ALBA POLLEN (UNII: VU8C8SB23P)
    • POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (Active Moiety)

    Which are Allergy New England Mix 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 Allergy New England Mix?

    * 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".