NDC 63083-4009 Mycobacter/mycoplasma Nosode 4009
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-4009?
What are the uses for Mycobacter/mycoplasma Nosode 4009?
Which are Mycobacter/mycoplasma Nosode 4009 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- SULFURIC ACID (UNII: O40UQP6WCF)
- SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
- MYCOBACTERIUM ABSCESSUS (UNII: Y9O4JH3X21)
- MYCOBACTERIUM ABSCESSUS (UNII: Y9O4JH3X21) (Active Moiety)
- MYCOBACTERIUM AVIUM (UNII: 67P4WI780Z)
- MYCOBACTERIUM AVIUM (UNII: 67P4WI780Z) (Active Moiety)
- MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS (UNII: XH0F4IP2RX)
- MYCOBACTERIUM AVIUM SUBSP. PARATUBERCULOSIS (UNII: XH0F4IP2RX) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
Which are Mycobacter/mycoplasma Nosode 4009 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".