NDC 63083-4001 Mycosis Nosode 4001
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-4001 - Mycosis Nosode
Product Packages
NDC Code 63083-4001-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-4001?
What are the uses for Mycosis Nosode 4001?
Which are Mycosis Nosode 4001 UNII Codes?
The UNII codes for the active ingredients in this product are:
- PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W)
- PLEOSPORA HERBARUM (UNII: 0N3Z1P4B2W) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- CANDIDA TORRESII (UNII: PH3OYJ624Q)
- CANDIDA TORRESII (UNII: PH3OYJ624Q) (Active Moiety)
- CANDIDA TROPICALIS (UNII: Q222J2186W)
- CANDIDA TROPICALIS (UNII: Q222J2186W) (Active Moiety)
- RHODOTORULA RUBRA (UNII: 15W81V867R)
- RHODOTORULA RUBRA (UNII: 15W81V867R) (Active Moiety)
- GEOTRICHUM CANDIDUM (UNII: 5964J742O8)
- GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (Active Moiety)
- MUCOR RACEMOSUS (UNII: 17RH99LQ7G)
- MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (Active Moiety)
- PENICILLIN G (UNII: Q42T66VG0C)
- PENICILLIN G (UNII: Q42T66VG0C) (Active Moiety)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (Active Moiety)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (Active Moiety)
Which are Mycosis Nosode 4001 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".