NDC 63083-3024 Connective Tissue Liquescence 3024
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-3024?
What are the uses for Connective Tissue Liquescence 3024?
Which are Connective Tissue Liquescence 3024 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BOVINE TYPE I COLLAGEN (SKIN) (UNII: 0127KU7397)
- BOVINE TYPE I COLLAGEN (SKIN) (UNII: 0127KU7397) (Active Moiety)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (Active Moiety)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- BOS TAURUS NERVE (UNII: 28G2U3MQJK)
- BOS TAURUS NERVE (UNII: 28G2U3MQJK) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- BOS TAURUS BONE MARROW (UNII: 08X0K2M57P)
- BOS TAURUS BONE MARROW (UNII: 08X0K2M57P) (Active Moiety)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- CONDOLIASE (UNII: 7SI2UZG934) (Active Moiety)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLUCOSAMINE (UNII: N08U5BOQ1K) (Active Moiety)
- MAGNESIUM (UNII: I38ZP9992A)
- MAGNESIUM (UNII: I38ZP9992A) (Active Moiety)
- MANGANESE (UNII: 42Z2K6ZL8P)
- MANGANESE (UNII: 42Z2K6ZL8P) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Connective Tissue Liquescence 3024 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)
* Please review the disclaimer below.
[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".