NDC 50181-0042 Biotox V Mmr
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 50181-0042?
What are the uses for Biotox V Mmr?
Which are Biotox V Mmr UNII Codes?
The UNII codes for the active ingredients in this product are:
- HORSERADISH (UNII: 8DS6G120HJ)
- HORSERADISH (UNII: 8DS6G120HJ) (Active Moiety)
- HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP)
- HUMAN HERPESVIRUS 3 (UNII: 9885M7D6JP) (Active Moiety)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (Active Moiety)
- MEASLES VIRUS (UNII: HT3R7C012Q)
- MEASLES VIRUS (UNII: HT3R7C012Q) (Active Moiety)
- JAPANESE ENCEPHALITIS VIRUS (UNII: P07E7XWU9D)
- JAPANESE ENCEPHALITIS VIRUS (UNII: P07E7XWU9D) (Active Moiety)
- MUMPS VIRUS (UNII: YF0S03R447)
- MUMPS VIRUS (UNII: YF0S03R447) (Active Moiety)
- RUBELLA VIRUS (UNII: U751HEX436)
- RUBELLA VIRUS (UNII: U751HEX436) (Active Moiety)
- POLIOVIRUS (UNII: FZJ641678T)
- POLIOVIRUS (UNII: FZJ641678T) (Active Moiety)
Which are Biotox V Mmr 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".