NDC 63083-2037 Large Joint Pain Drops 2037
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What is NDC 63083-2037?
What are the uses for Large Joint Pain Drops 2037?
Which are Large Joint Pain Drops 2037 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- SULFURIC ACID (UNII: O40UQP6WCF)
- SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (Active Moiety)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ) (Active Moiety)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8) (Active Moiety)
Which are Large Joint Pain Drops 2037 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".