NDC 63083-4002 Bacterial Nosode 4002
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-4002 - Bacterial Nosode
Product Packages
NDC Code 63083-4002-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-4002?
What are the uses for Bacterial Nosode 4002?
Which are Bacterial Nosode 4002 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
- DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN (UNII: 50SG618FGN)
- DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN (UNII: 50SG618FGN) (Active Moiety)
- STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98)
- STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98) (Active Moiety)
- PROTEUS VULGARIS (UNII: 11T9HCO30O)
- PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
- SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
- JUSTICIA SPICIGERA LEAF (UNII: 2A6D37HK4A)
- JUSTICIA SPICIGERA LEAF (UNII: 2A6D37HK4A) (Active Moiety)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004)
- STAPHYLOCOCCUS AUREUS (UNII: O478WX4004) (Active Moiety)
- BOVINE TUBERCULIN (UNII: HKD62G79N5)
- BOVINE TUBERCULIN (UNII: HKD62G79N5) (Active Moiety)
Which are Bacterial Nosode 4002 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".