NDC 50211-001 Hemo Fin
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What is NDC 50211-001?
What are the uses for Hemo Fin?
Which are Hemo Fin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Hemo Fin 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- IODINE (UNII: 9679TC07X4)
- OKRA (UNII: 51ME2L7STL)
- OLEIC ACID (UNII: 2UMI9U37CP)
- SAGE (UNII: 065C5D077J)
What is the NDC to RxNorm Crosswalk for Hemo Fin?
- RxCUI: 1540838 - petrolatum 93.3 % Rectal Ointment
- RxCUI: 1540838 - petrolatum 0.933 MG/MG Rectal Ointment
- RxCUI: 1540843 - Hemo-Fin 93.3 % Rectal Ointment
- RxCUI: 1540843 - petrolatum 0.933 MG/MG Rectal Ointment [Hemo-Fin]
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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".