NDC 63083-2070 Anti-rheumatic Formula 2070
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2070 - Anti-rheumatic Formula
Product Packages
NDC Code 63083-2070-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2070?
What are the uses for Anti-rheumatic Formula 2070?
Which are Anti-rheumatic Formula 2070 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM CARMICHAELI LATERAL ROOT (UNII: 2A9PW94VJX)
- ACONITUM CARMICHAELI LATERAL ROOT (UNII: 2A9PW94VJX) (Active Moiety)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- FRANKINCENSE (UNII: R9XLF1R1WM) (Active Moiety)
- SOLANUM NIGRUM TOP (UNII: O4G5C1G3W5)
- SOLANUM NIGRUM TOP (UNII: O4G5C1G3W5) (Active Moiety)
- MYRRH (UNII: JC71GJ1F3L)
- MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
- ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)
- ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30) (Active Moiety)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3)
- SUS SCROFA LUNG (UNII: 7GL3G1COB3) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
Which are Anti-rheumatic Formula 2070 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".