NDC 50181-0062 Biotox VI

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50181-0062
Proprietary Name:
Biotox VI
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Wellness Center For Research And Education, Inc.
Labeler Code:
50181
Start Marketing Date: [9]
03-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 50181-0062-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 50181-0062?

The NDC code 50181-0062 is assigned by the FDA to the product Biotox VI which is product labeled by The Wellness Center For Research And Education, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50181-0062-1 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 Biotox VI?

Fatigue, fever, cough, flu-like symptoms, heart palpitations, virus, pain, swelling and stiffness of limbs. Fatigue, fever, cough, flu-like symptoms, heart palpitations, virus, pain, swelling and stiffness of limbs.

Which are Biotox VI UNII Codes?

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

  • HORSERADISH (UNII: 8DS6G120HJ)
  • HORSERADISH (UNII: 8DS6G120HJ) (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)
  • INFLUENZA A VIRUS A/BRISBANE/02/2018 IVR-190 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: XW4JB03TI5)
  • INFLUENZA A VIRUS A/BRISBANE/02/2018 IVR-190 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 92XE6GHC89) (Active Moiety)
  • INFLUENZA A VIRUS A/KANSAS/14/2017 X-327 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 3NZW5ND3D6)
  • INFLUENZA A VIRUS A/KANSAS/14/2017 X-327 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: K329YCD1N9) (Active Moiety)
  • INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 8V4458342X)
  • INFLUENZA B VIRUS B/MARYLAND/15/2016 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: OES3CXI7E9) (Active Moiety)
  • MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
  • MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
  • HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
  • HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
  • HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J)
  • HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (Active Moiety)
  • HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD)
  • HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD) (Active Moiety)
  • HUMAN COXSACKIEVIRUS B4 (UNII: FYF75V7FDY)
  • HUMAN COXSACKIEVIRUS B4 (UNII: FYF75V7FDY) (Active Moiety)
  • STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
  • STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
  • HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
  • HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)

Which are Biotox VI 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:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".