NDC 48951-8116 Quercus Borago Hemorrhoid Relief
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 48951-8116?
What are the uses for Quercus Borago Hemorrhoid Relief?
Which are Quercus Borago Hemorrhoid Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W)
- QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (Active Moiety)
- MERCURIALIS PERENNIS (UNII: Q35465A1MA)
- MERCURIALIS PERENNIS (UNII: Q35465A1MA) (Active Moiety)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- BORAGE (UNII: PB618V0K2W)
- BORAGE (UNII: PB618V0K2W) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- ANTIMONY (UNII: 9IT35J3UV3)
- ANTIMONY (UNII: 9IT35J3UV3) (Active Moiety)
Which are Quercus Borago Hemorrhoid Relief 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:
- OLIVE OIL (UNII: 6UYK2W1W1E)
- WATER (UNII: 059QF0KO0R)
- LANOLIN (UNII: 7EV65EAW6H)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MINERAL OIL (UNII: T5L8T28FGP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
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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".