NDC 43857-0555 Osteoplex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 43857-0555?
What are the uses for Osteoplex?
Which are Osteoplex UNII Codes?
The UNII codes for the active ingredients in this product are:
- EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25)
- EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- MANGANESE CHLORIDE (UNII: QQE170PANO)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SUS SCROFA PARATHYROID GLAND (UNII: 2KBE35NE8S)
- SUS SCROFA PARATHYROID GLAND (UNII: 2KBE35NE8S) (Active Moiety)
- SUS SCROFA LIGAMENT (UNII: 2004Q810JO)
- SUS SCROFA LIGAMENT (UNII: 2004Q810JO) (Active Moiety)
Which are Osteoplex 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".