NDC 59779-997 Cvs Hemorrhoidal Topical Analgesic
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What is NDC 59779-997?
What are the uses for Cvs Hemorrhoidal Topical Analgesic?
Which are Cvs Hemorrhoidal Topical Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIBUCAINE (UNII: L6JW2TJG99)
- DIBUCAINE (UNII: L6JW2TJG99) (Active Moiety)
Which are Cvs Hemorrhoidal Topical Analgesic 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:
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- WATER (UNII: 059QF0KO0R)
- LANOLIN (UNII: 7EV65EAW6H)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
What is the NDC to RxNorm Crosswalk for Cvs Hemorrhoidal Topical Analgesic?
- RxCUI: 238784 - dibucaine 1 % Rectal Ointment
- RxCUI: 238784 - dibucaine 0.01 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".