NDC 52919-123 Lymphomyosot
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Product Details
What is NDC 52919-123?
Which are Lymphomyosot UNII Codes?
The UNII codes for the active ingredients in this product are:
- GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL)
- GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL) (Active Moiety)
- RORIPPA NASTURTIUM-AQUATICUM (UNII: YH89GMV676)
- RORIPPA NASTURTIUM-AQUATICUM (UNII: YH89GMV676) (Active Moiety)
- FERROUS IODIDE (UNII: F5452U54PN)
- FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
- TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
- VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J)
- VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (Active Moiety)
- EQUISETUM HYEMALE (UNII: 59677RXH25)
- EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PINUS SYLVESTRIS TOP (UNII: Q1RGP4UB73)
- PINUS SYLVESTRIS TOP (UNII: Q1RGP4UB73) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
- ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
- SARSAPARILLA (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- LEVOTHYROXINE (UNII: Q51BO43MG4)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
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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".