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  4. NDC Product Code: 50181-0075 Biotox Bac I

NDC 50181-0075 Biotox Bac I

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50181-0075?
  4. Biotox Bac I Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50181-0075
Proprietary Name:
Biotox Bac I
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Wellness Center For Research
Labeler Code:
50181
Product Label ID:
df12608a-d29e-4c95-ac06-bbf2c38ba007
Start Marketing Date: [9]
05-04-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 50181-0075?

The NDC code 50181-0075 is assigned by the FDA to the product Biotox Bac I which is product labeled by The Wellness Center For Research. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50181-0075-1 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 Bac I?

Tired, rash, flu-like symptoms, swelling, joint pain, tingling, numbness in your hands, feet or back, brain fog, poor memory, weakness or paralysis in facial muscles. Tired, rash, flu-like symptoms, swelling, joint pain, tingling, numbness in your hands, feet or back, brain fog, poor memory, weakness or paralysis in facial muscles.

Which are Biotox Bac I UNII Codes?

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

Which are Biotox Bac I 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".