NDC 43406-0131 Cardio Hp
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43406-0131?
What are the uses for Cardio Hp?
Which are Cardio Hp UNII Codes?
The UNII codes for the active ingredients in this product are:
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW)
- DIGITALIS PURPUREA WHOLE (UNII: UD4O8TY7RW) (Active Moiety)
- LYCOPUS VIRGINICUS (UNII: TWH5125Q6F)
- LYCOPUS VIRGINICUS (UNII: TWH5125Q6F) (Active Moiety)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PULSATILLA PATENS (UNII: 4M1169RWJD)
- ANEMONE PATENS (UNII: 4M1169RWJD) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
Which are Cardio 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".