NDC 63083-3020 Cartilage Liquescence 3020
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What is NDC 63083-3020?
What are the uses for Cartilage Liquescence 3020?
Which are Cartilage Liquescence 3020 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- STRYCHNOS WALLICHIANA WHOLE (UNII: 37O494C4B6)
- STRYCHNOS WALLICHIANA WHOLE (UNII: 37O494C4B6) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ) (Active Moiety)
- SHARK CARTILAGE (UNII: D2YCN1I522)
- SHARK CARTILAGE (UNII: D2YCN1I522) (Active Moiety)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ARSENIC TRIBROMIDE (UNII: 41CN475O7F)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- THYMOL (UNII: 3J50XA376E)
- THYMOL (UNII: 3J50XA376E) (Active Moiety)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
Which are Cartilage Liquescence 3020 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".