NDC 63083-4030 Tick Pathogen Nosode 4030
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What is NDC 63083-4030?
What are the uses for Tick Pathogen Nosode 4030?
Which are Tick Pathogen Nosode 4030 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANAPLASMA PHAGOCYTOPHILUM (UNII: BHE5668847)
- ANAPLASMA PHAGOCYTOPHILUM (UNII: BHE5668847) (Active Moiety)
- BABESIA MICROTI (UNII: 1948X6KEG3)
- BABESIA MICROTI (UNII: 1948X6KEG3) (Active Moiety)
- BARTONELLA HENSELAE (UNII: 84PG7W9845)
- BARTONELLA HENSELAE (UNII: 84PG7W9845) (Active Moiety)
- BORRELIA AFZELII (UNII: S7B7C89JD6)
- BORRELIA AFZELII (UNII: S7B7C89JD6) (Active Moiety)
- BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8)
- BORRELIA BURGDORFERI (UNII: 0J8NV9V5Q8) (Active Moiety)
- VIOLA JAPONICA WHOLE (UNII: N20DAF8188)
- VIOLA JAPONICA WHOLE (UNII: N20DAF8188) (Active Moiety)
- EHRLICHIA CHAFFEENSIS (UNII: 5ERQ90UTGC)
- EHRLICHIA CHAFFEENSIS (UNII: 5ERQ90UTGC) (Active Moiety)
- HUMAN HERPESVIRUS 6 (UNII: 4IX4VP35CR)
- HUMAN HERPESVIRUS 6 (UNII: 4IX4VP35CR) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- COXIELLA BURNETII (UNII: GRY5SDU86N)
- COXIELLA BURNETII (UNII: GRY5SDU86N) (Active Moiety)
- RICKETTSIA RICKETTSII (UNII: V6ZO3M43L5)
- RICKETTSIA RICKETTSII (UNII: V6ZO3M43L5) (Active Moiety)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H)
- FRANCISELLA TULARENSIS (UNII: NNR1301B0H) (Active Moiety)
Which are Tick Pathogen Nosode 4030 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
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[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".