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  4. NDC Product Code: 83027-0022 Fatigue Formula

NDC 83027-0022 Fatigue Formula

Medulla Ossis Suis,Spleen (bovine),Thymus (bovine),Carcinosin,Cytomegalovirus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83027-0022?
  4. Fatigue Formula Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
83027-0022
Proprietary Name:
Fatigue Formula
Non-Proprietary Name: [1]
Medulla Ossis Suis, Spleen (bovine), Thymus (bovine), Carcinosin, Cytomegalovirus Nosode, Influenzinum (2022-2023), Streptococcus Viridans, Toxoplasma Gondii, Epstein-bar Virus Nosode
Substance Name: [2]
Bos Taurus Spleen; Bos Taurus Thymus; Human Breast Tumor Cell; Human Herpesvirus 4; Human Herpesvirus 5; Influenza A Virus A/darwin/9/2021 Ivr-228 (h3n2) Antigen (uv, Formaldehyde Inactivated); Influenza A Virus A/victoria/2570/2019 Ivr-215 (h1n1) Antigen (uv, Formaldehyde Inactivated); Influenza B Virus B/austria/1359417/2021 Bvr-26 Antigen (uv, Formaldehyde Inactivated); Influenza B Virus B/phuket/3073/2013 Antigen (uv, Formaldehyde Inactivated); Streptococcus Viridans Group; Sus Scrofa Bone Marrow; Toxoplasma Gondii
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Nutritional Specialties, Inc.
    Labeler Code:
    83027
    Product Label ID:
    eaec858d-6a86-403a-b07b-62d7bd4fca4a
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-13-2023
    End Marketing Date: [10]
    08-02-2028
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 83027-0022-1

    Package Description: 60 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 83027-0022?

    The NDC code 83027-0022 is assigned by the FDA to the product Fatigue Formula which is a human over the counter drug product labeled by Nutritional Specialties, Inc.. The generic name of Fatigue Formula is medulla ossis suis, spleen (bovine), thymus (bovine), carcinosin, cytomegalovirus nosode, influenzinum (2022-2023), streptococcus viridans, toxoplasma gondii, epstein-bar virus nosode. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 83027-0022-1 60 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 Fatigue Formula?

    Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

    What are Fatigue Formula 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 Fatigue Formula UNII Codes?

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

    • SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
    • SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
    • BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
    • BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
    • BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
    • BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
    • HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
    • HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)
    • HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
    • HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
    • INFLUENZA A VIRUS A/VICTORIA/2570/2019 IVR-215 (H1N1) ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: 34C49NV47P)
    • INFLUENZA A VIRUS A/VICTORIA/2570/2019 IVR-215 (H1N1) HEMAGGLUTININ ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: NGL844Y7X6) (Active Moiety)
    • INFLUENZA A VIRUS A/DARWIN/9/2021 IVR-228 (H3N2) ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: P483J7GX6D)
    • INFLUENZA A VIRUS A/DARWIN/9/2021 IVR-228 (H3N2) HEMAGGLUTININ ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: GRN94TP8YV) (Active Moiety)
    • INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: TBV2PPG6EF)
    • INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 HEMAGGLUTININ ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: 28EAH8253X) (Active Moiety)
    • INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: H2198F8ZNA)
    • INFLUENZA B VIRUS B/PHUKET/3073/2013 HEMAGGLUTININ ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: 3VSF1BF3SR) (Active Moiety)
    • STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR)
    • STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR) (Active Moiety)
    • TOXOPLASMA GONDII (UNII: BMV90JF469)
    • TOXOPLASMA GONDII (UNII: BMV90JF469) (Active Moiety)
    • HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX)
    • HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (Active Moiety)

    Which are Fatigue Formula 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.

    [10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

    [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".