NDC 63083-3011 Herbal Diuretic Liquescence 3011
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-3011?
What are the uses for Herbal Diuretic Liquescence 3011?
Which are Herbal Diuretic Liquescence 3011 UNII Codes?
The UNII codes for the active ingredients in this product are:
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- ANTIMONY CATION (3+) (UNII: 069647RPT5)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- GARLIC (UNII: V1V998DC17)
- GARLIC (UNII: V1V998DC17) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G)
- RAUWOLFIA SERPENTINA (UNII: H192N84N1G) (Active Moiety)
- RENIN (UNII: 2MS130CE0A)
- RENIN (UNII: 2MS130CE0A) (Active Moiety)
- BOS TAURUS ARTERY (UNII: R2M88A4HSI)
- BOS TAURUS ARTERY (UNII: R2M88A4HSI) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- MIDORIAMIN (UNII: FB29QPB7US)
- MIDORIAMIN (UNII: FB29QPB7US) (Active Moiety)
Which are Herbal Diuretic Liquescence 3011 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".