NDC 50181-0056 Biotox Lyme
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center For Research And Education, Inc.
- 50181-0056 - Biotox Lyme
Product Packages
NDC Code 50181-0056-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50181-0056?
What are the uses for Biotox Lyme?
Which are Biotox Lyme UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8)
- BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8) (Active Moiety)
- EHRLICHIA CANIS (UNII: 970Y8T1JZY)
- EHRLICHIA CANIS (UNII: 970Y8T1JZY) (Active Moiety)
- BABESIA MICROTI (UNII: 1948X6KEG3)
- BABESIA MICROTI (UNII: 1948X6KEG3) (Active Moiety)
- COXIELLA BURNETII (UNII: GRY5SDU86N)
- COXIELLA BURNETII (UNII: GRY5SDU86N) (Active Moiety)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP)
- HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP) (Active Moiety)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H) (Active Moiety)
- RICKETTSIA PROWAZEKII (UNII: TVS414L9M5)
- RICKETTSIA PROWAZEKII (UNII: TVS414L9M5) (Active Moiety)
Which are Biotox Lyme 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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".