NDC 63083-4018 Toxic Fungi-mold Nosode 4018
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-4018?
What are the uses for Toxic Fungi-mold Nosode 4018?
Which are Toxic Fungi-mold Nosode 4018 UNII Codes?
The UNII codes for the active ingredients in this product are:
- PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W)
- PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (Active Moiety)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (Active Moiety)
- CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A)
- CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (Active Moiety)
- CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R)
- CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (Active Moiety)
- RHODOTORULA RUBRA (UNII: 15W81V867R)
- RHODOTORULA RUBRA (UNII: 15W81V867R) (Active Moiety)
- HELMINTHOSPORIUM CARBONUM TOXIN I (UNII: 17NL0QLS6P)
- HELMINTHOSPORIUM CARBONUM TOXIN I (UNII: 17NL0QLS6P) (Active Moiety)
- HISTOPLASMA CAPSULATUM (UNII: 6EF1RL8Z5O)
- HISTOPLASMA CAPSULATUM (UNII: 6EF1RL8Z5O) (Active Moiety)
- PENICILLIN G (UNII: Q42T66VG0C)
- PENICILLIN G (UNII: Q42T66VG0C) (Active Moiety)
- STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP)
- STACHYBOTRYS CHARTARUM (UNII: HJ4L70T1ZP) (Active Moiety)
Which are Toxic Fungi-mold Nosode 4018 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)
* 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".