NDC 83027-0022 Fatigue Formula
Medulla Ossis Suis, Spleen (bovine), Thymus (bovine), Carcinosin, Cytomegalovirus Noso...

Product Information

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, RxNorm crosswalk and the complete product label.

NDC Product Code83027-0022
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Fatigue Formula
Non-Proprietary Name 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.
Medulla Ossis Suis, Spleen (bovine), Thymus (bovine), Carcinosin, Cytomegalovirus Nosode, Influenzinum (2022-2023), Streptococcus Viridans, Toxoplasma Gondii, Epstein-bar Virus Nosode
Product Type 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.
Human Otc Drug
Dosage FormSpray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Nutritional Specialties, Inc.
Labeler Code83027
Marketing Category 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
03-13-2023
Listing Expiration Date 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.
12-31-2024
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Fatigue Formula?


Product Packages

NDC Code 83027-0022-1

Package Description: 60 mL in 1 BOTTLE, SPRAY

Product Details

What are Fatigue Formula Active Ingredients?

Fatigue Formula Active Ingredients UNII Codes

  • 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)

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.

* Please review the disclaimer below.

Fatigue Formula Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredients:



Medulla Ossis Suis 6X, 12X, 30X, Spleen 6X, 12X, 30X, Thymus 6X, 12X, 30X, Carcinosin 16X, 24X, 30X, 100X, Cytomegalovirus Nosode 16X, 24X, 30X, 100X, Influenzinum 16X, 24X, 30X, 100X, Streptococcus Viridans 16X, 24X, 30X, 100X, Toxoplasma Gondii 16X, 24X, 30X, 100X, Epstein-Bar Virus Nosode 16C, 24C, 30C, 100C.


Purpose:



Assists in temporary relief of fatigue and headaches.†

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


Warnings:



Professional Use Only

If pregnant or breast-feeding, ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

If condition worsens, seek medical attention.

KEEP OUT OF REACH OF CHILDREN

Do not use if tamper evident seal is broken or missing.

Store in a cool place after opening


Keep Out Of Reach Of Children:



KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control Center right away.


Directions:



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.


Indications:



Assists in temporary relief of fatigue and headaches.†

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


Inactive Ingredients:



Alcohol USP 20%, Purified Water USP.


Questions:



MANUFACTURED EXCLUSIVELY FOR

NUTRITIONAL SPECIALTIES, INC.

PO BOX 97227

PITTSBURG, PA 15229

www.phpltd.com


Package Label Display:



Professional

Health Products

HOMEOPATHIC

NDC 83027-0022-1

FATIGUE

FORMULA

2 FL. OZ (60 ml)


* Please review the disclaimer below.