NDC 65923-777 Shopko Hemorrhoidal
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 65923-777?
What are the uses for Shopko Hemorrhoidal?
Which are Shopko Hemorrhoidal UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINERAL OIL (UNII: T5L8T28FGP)
- MINERAL OIL (UNII: T5L8T28FGP) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- SHARK LIVER OIL (UNII: 4B24275HEU)
- SHARK LIVER OIL (UNII: 4B24275HEU) (Active Moiety)
Which are Shopko 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:
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- THYME OIL (UNII: 2UK410MY6B)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Shopko Hemorrhoidal?
- RxCUI: 1544968 - mineral oil 14 % / petrolatum 71.9 % / phenylephrine HCl 0.25 % / shark liver oil preparation 3 % Rectal Ointment
- RxCUI: 1544968 - mineral oil 0.14 MG/MG / petrolatum 0.719 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG / shark liver oil 0.03 MG/MG Rectal Ointment
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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".