NDC 44911-0596 Urinary Hp
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 44911-0596?
What are the uses for Urinary Hp?
Which are Urinary Hp UNII Codes?
The UNII codes for the active ingredients in this product are:
- SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z)
- CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- TURPENTINE OIL (UNII: C5H0QJ6V7F)
- TURPENTINE OIL (UNII: C5H0QJ6V7F) (Active Moiety)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID) (Active Moiety)
- POPULUS TREMULOIDES LEAF (UNII: 7IIH57D9E0)
- POPULUS TREMULOIDES LEAF (UNII: 7IIH57D9E0) (Active Moiety)
Which are Urinary 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)
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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".