NDC 63083-5015 Muscle/ligament/cartilage Drops 5015
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-5015 - Muscle/ligament/cartilage Drops
Product Packages
NDC Code 63083-5015-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-5015?
What are the uses for Muscle/ligament/cartilage Drops 5015?
Which are Muscle/ligament/cartilage Drops 5015 UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLUCOSAMINE (UNII: N08U5BOQ1K) (Active Moiety)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
- LEVOCARNITINE (UNII: 0G389FZZ9M) (Active Moiety)
- ORNITHINE (UNII: E524N2IXA3)
- ORNITHINE (UNII: E524N2IXA3) (Active Moiety)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ) (Active Moiety)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- CONDOLIASE (UNII: 7SI2UZG934) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8) (Active Moiety)
Which are Muscle/ligament/cartilage Drops 5015 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".