NDC 54868-5876 Zeasorb AF
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Product Details
What is NDC 54868-5876?
What are the uses for Zeasorb AF?
Which are Zeasorb AF UNII Codes?
The UNII codes for the active ingredients in this product are:
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (Active Moiety)
Which are Zeasorb AF 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:
- ACRYLAMIDE (UNII: 20R035KLCI)
- ALDIOXA (UNII: 8T66I31YNK)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- IMIDUREA (UNII: M629807ATL)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Zeasorb AF?
- RxCUI: 1437793 - Zeasorb 2 % Topical Powder
- RxCUI: 1437793 - miconazole nitrate 0.02 MG/MG Topical Powder [Zeasorb]
- RxCUI: 1437793 - Zeasorb 0.02 MG/MG Topical Powder
- RxCUI: 998461 - miconazole nitrate 2 % Topical Powder
- RxCUI: 998461 - miconazole nitrate 0.02 MG/MG Topical Powder
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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".