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  4. NDC Product Code: 44911-0324 Flower Antigens

NDC 44911-0324 Flower Antigens

Arsenicum Album,Lycopodium Clavatum,Pulsatilla (pratensis),Bellis Perennis,Calendula - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0324?
  4. Flower Antigens Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
44911-0324
Proprietary Name:
Flower Antigens
Non-Proprietary Name: [1]
Arsenicum Album, Lycopodium Clavatum, Pulsatilla (pratensis), Bellis Perennis, Calendula Officinalis, Camellia Japonica, Chrysanthemum Coronarium, Chrysanthemum Leucanthemum, Convallaria Majalis, Gardenia Jasminoides, Impatiens Glandulifera, Flos, Iris Tenax, Lilium Tigrinum, Narcissus Pseudo-narcissus, Rosa Damascena, Syringa Vulgaris
Substance Name: [2]
Arsenic Trioxide; Bellis Perennis Whole; Calendula Officinalis Flowering Top; Camellia Japonica Flower; Convallaria Majalis; Gardenia Jasminoides Flower; Glebionis Coronaria Whole; Impatiens Glandulifera Flower; Iris Tenax Whole; Leucanthemum Vulgare Whole; Lilium Lancifolium Whole Flowering; Lycopodium Clavatum Spore; Narcissus Pseudonarcissus Flower; Pulsatilla Pratensis Whole; Rosa Damascena Flowering Top; Syringa Vulgaris Flower
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]
    Energique, Inc.
    Labeler Code:
    44911
    Product Label ID:
    d4a73c9e-242a-4270-bf7c-36427cf57632
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    07-08-2016
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 44911-0324?

    The NDC code 44911-0324 is assigned by the FDA to the product Flower Antigens which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Flower Antigens is arsenicum album, lycopodium clavatum, pulsatilla (pratensis), bellis perennis, calendula officinalis, camellia japonica, chrysanthemum coronarium, chrysanthemum leucanthemum, convallaria majalis, gardenia jasminoides, impatiens glandulifera, flos, iris tenax, lilium tigrinum, narcissus pseudo-narcissus, rosa damascena, syringa vulgaris. 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 44911-0324-1 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 Flower Antigens?

    May temporarily relieve symptoms associated with flower allergies.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with flower allergies.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

    What are Flower Antigens 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 Flower Antigens UNII Codes?

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

    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
    • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
    • ANEMONE PRATENSIS (UNII: 8E272251DI)
    • ANEMONE PRATENSIS (UNII: 8E272251DI) (Active Moiety)
    • BELLIS PERENNIS (UNII: 2HU33I03UY)
    • BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
    • CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF) (Active Moiety)
    • GLEBIONIS CORONARIA WHOLE (UNII: 812HCC9672)
    • GLEBIONIS CORONARIA WHOLE (UNII: 812HCC9672) (Active Moiety)
    • LEUCANTHEMUM VULGARE (UNII: 744CCZ722D)
    • LEUCANTHEMUM VULGARE (UNII: 744CCZ722D) (Active Moiety)
    • CONVALLARIA MAJALIS (UNII: QHH4HVF5QE)
    • CONVALLARIA MAJALIS (UNII: QHH4HVF5QE) (Active Moiety)
    • GARDENIA JASMINOIDES FLOWER (UNII: 2TU49609L2)
    • GARDENIA JASMINOIDES FLOWER (UNII: 2TU49609L2) (Active Moiety)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
    • IRIS TENAX (UNII: Z34X58O70B)
    • IRIS TENAX (UNII: Z34X58O70B) (Active Moiety)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
    • NARCISSUS PSEUDONARCISSUS FLOWER (UNII: L879RBF1WN)
    • NARCISSUS PSEUDONARCISSUS FLOWER (UNII: L879RBF1WN) (Active Moiety)
    • ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G)
    • ROSA DAMASCENA FLOWERING TOP (UNII: 21W82Q764G) (Active Moiety)
    • SYRINGA VULGARIS FLOWER (UNII: 9V5O040S3W)
    • SYRINGA VULGARIS FLOWER (UNII: 9V5O040S3W) (Active Moiety)

    Which are Flower Antigens 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".