NDC 63083-9405 Parasite Nosode Combination 9405
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-9405 - Parasite Nosode Combination
Product Packages
NDC Code 63083-9405-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-9405?
What are the uses for Parasite Nosode Combination 9405?
Which are Parasite Nosode Combination 9405 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT)
- ARTEMISIA CINA PRE-FLOWERING TOP (UNII: 28M1820ACT) (Active Moiety)
- BAPTISIA TINCTORIA WHOLE (UNII: 5K1UO2888Y)
- BAPTISIA TINCTORIA WHOLE (UNII: 5K1UO2888Y) (Active Moiety)
- TEUCRIUM MARUM WHOLE (UNII: 10464S0TAA)
- TEUCRIUM MARUM WHOLE (UNII: 10464S0TAA) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- SPIGELIA MARILANDICA ROOT (UNII: 467D26HS0B)
- SPIGELIA MARILANDICA ROOT (UNII: 467D26HS0B) (Active Moiety)
- TRICHINELLA SPIRALIS (UNII: 2PYI6D7HCQ)
- TRICHINELLA SPIRALIS (UNII: 2PYI6D7HCQ) (Active Moiety)
Which are Parasite Nosode Combination 9405 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".