NDC 55741-412 Nupercainal Bio-active Hemorrhoidal
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 55741-412?
What are the uses for Nupercainal Bio-active Hemorrhoidal?
Which are Nupercainal Bio-active Hemorrhoidal UNII Codes?
The UNII codes for the active ingredients in this product are:
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
Which are Nupercainal Bio-active Hemorrhoidal 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- PARAFFIN (UNII: I9O0E3H2ZE)
- LANOLIN (UNII: 7EV65EAW6H)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MENTHOL (UNII: L7T10EIP3A)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
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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".