NDC 63083-9312 Bridged Phenyl Combination 9312
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-9312 - Bridged Phenyl Combination
Product Packages
NDC Code 63083-9312-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-9312?
What are the uses for Bridged Phenyl Combination 9312?
Which are Bridged Phenyl Combination 9312 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN) (Active Moiety)
- BOS TAURUS BILE (UNII: ET3651ZLOU)
- BOS TAURUS BILE (UNII: ET3651ZLOU) (Active Moiety)
- PROXIFEZONE (UNII: 005MKH0F6D)
- PROXIFEZONE (UNII: 005MKH0F6D) (Active Moiety)
- PROPHAM (UNII: Y647G714RY)
- PROPHAM (UNII: Y647G714RY) (Active Moiety)
- SODIUM (UNII: 9NEZ333N27)
- SODIUM (UNII: 9NEZ333N27) (Active Moiety)
- 3'-METHYLPHTHALANILIC ACID (UNII: 3R15BUY339)
- 3'-METHYLPHTHALANILIC ACID (UNII: 3R15BUY339) (Active Moiety)
Which are Bridged Phenyl Combination 9312 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".