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  4. NDC Product Code: 42731-081 Triple Flu Defense

NDC 42731-081 Triple Flu Defense

Homeopathic Flu Defense Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42731-081?
  4. Triple Flu Defense Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
42731-081
Proprietary Name:
Triple Flu Defense
Non-Proprietary Name: [1]
Homeopathic Flu Defense
Substance Name: [2]
Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Calcium Sulfide; Cinchona Officinalis Bark; Eupatorium Perfoliatum Flowering Top; Gelsemium Sempervirens Root; Influenza A Virus A/brisbane/02/2018 (h1n1) Recombinant Hemagglutinin Antigen; Influenza A Virus A/kansas/14/2017 (h3n2) Recombinant Hemagglutinin Antigen; Influenza B Virus B/colorado/06/2017 Live (attenuated) Antigen; Influenza B Virus B/phuket/3073/2013 Recombinant Hemagglutinin Antigen; Ipecac; Oyster Shell Calcium Carbonate, Crude; Phosphoric Acid; Phosphorus; Phytolacca Dodecandra Whole
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]
    Nenningers Naturals, Llc
    Labeler Code:
    42731
    Product Label ID:
    fed139a8-55d3-8a7c-e053-6294a90afb51
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    08-01-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 42731-081?

    The NDC code 42731-081 is assigned by the FDA to the product Triple Flu Defense which is a human over the counter drug product labeled by Nenningers Naturals, Llc. The generic name of Triple Flu Defense is homeopathic flu defense. 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 42731-081-01 1 bottle, dropper in 1 carton / 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 Triple Flu Defense?

    At the first sign of the flu take 3 times per day for symptom relief and once per week for maintenance.Place drops on tongue or mix with one ounce of water.Adult Dose is 20 drops per dose. Children under 12 take 2 drops for every 10 pounds of body weight up to a maximum of 20 drops per dose.

    What are Triple Flu Defense 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 Triple Flu Defense UNII Codes?

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

    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
    • PHYTOLACCA DODECANDRA WHOLE (UNII: UIK887RM3Z)
    • PHYTOLACCA DODECANDRA WHOLE (UNII: UIK887RM3Z) (Active Moiety)
    • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
    • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
    • IPECAC (UNII: 62I3C8233L)
    • IPECAC (UNII: 62I3C8233L) (Active Moiety)
    • PHOSPHORUS (UNII: 27YLU75U4W)
    • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
    • PHOSPHORIC ACID (UNII: E4GA8884NN)
    • PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
    • INFLUENZA A VIRUS A/BRISBANE/02/2018 (H1N1) RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: DC4ELG1BFZ)
    • INFLUENZA A VIRUS A/BRISBANE/02/2018 (H1N1) RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: DC4ELG1BFZ) (Active Moiety)
    • INFLUENZA A VIRUS A/KANSAS/14/2017 (H3N2) RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: I282A48KKK)
    • INFLUENZA A VIRUS A/KANSAS/14/2017 (H3N2) RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: I282A48KKK) (Active Moiety)
    • INFLUENZA B VIRUS B/COLORADO/06/2017 LIVE (ATTENUATED) ANTIGEN (UNII: RS6978S7U6)
    • INFLUENZA B VIRUS B/COLORADO/06/2017 LIVE (ATTENUATED) ANTIGEN (UNII: RS6978S7U6) (Active Moiety)
    • INFLUENZA B VIRUS B/PHUKET/3073/2013 RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: POQ8DQO9S3)
    • INFLUENZA B VIRUS B/PHUKET/3073/2013 RECOMBINANT HEMAGGLUTININ ANTIGEN (UNII: POQ8DQO9S3) (Active Moiety)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
    • CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
    • CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)

    Which are Triple Flu Defense 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".