NDC 43406-0034 Osteoporosis Hp
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43406-0034?
What are the uses for Osteoporosis Hp?
Which are Osteoporosis Hp UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ) (Active Moiety)
- HEKLA LAVA (UNII: C21158IIRK)
- HEKLA LAVA (UNII: C21158IIRK) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- COMFREY LEAF (UNII: DG4F8T839X)
- COMFREY LEAF (UNII: DG4F8T839X) (Active Moiety)
Which are Osteoporosis Hp 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".