NDC 63083-2039 Kidney Stone Drops 2039
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2039?
What are the uses for Kidney Stone Drops 2039?
Which are Kidney Stone Drops 2039 UNII Codes?
The UNII codes for the active ingredients in this product are:
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36)
- HAWTHORN LEAF WITH FLOWER (UNII: 6OM09RPY36) (Active Moiety)
- DIGITALIS (UNII: F1T8QT9U8B)
- DIGITALIS (UNII: F1T8QT9U8B) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- OXALIC ACID (UNII: 9E7R5L6H31)
- OXALIC ACID (UNII: 9E7R5L6H31) (Active Moiety)
- URIC ACID (UNII: 268B43MJ25)
- URIC ACID (UNII: 268B43MJ25) (Active Moiety)
Which are Kidney Stone Drops 2039 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)
* 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".