NDC 63083-4024 Low Vaccinosis Nosode 4024
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-4024 - Low Vaccinosis Nosode
Product Packages
NDC Code 63083-4024-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-4024?
What are the uses for Low Vaccinosis Nosode 4024?
Which are Low Vaccinosis Nosode 4024 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
- LAURTRIMONIUM BROMIDE (UNII: 6IC8NZ97S2)
- LAURTRIMONIUM BROMIDE (UNII: 6IC8NZ97S2) (Active Moiety)
- MUMPS VIRUS (UNII: YF0S03R447)
- MUMPS VIRUS (UNII: YF0S03R447) (Active Moiety)
- CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: K3W1N8YP13)
- CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: K3W1N8YP13) (Active Moiety)
- ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U)
- ANGUILLA ROSTRATA BLOOD SERUM (UNII: L7B16ESD1U) (Active Moiety)
- SERUM, HORSE (UNII: QHD0E51VON)
- SERUM, HORSE (UNII: QHD0E51VON) (Active Moiety)
Which are Low Vaccinosis Nosode 4024 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".