NDC 54868-6246 Vusion
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6246 - Vusion
Product Packages
NDC Code 54868-6246-0
Package Description: 50 g in 1 TUBE
Product Details
What is NDC 54868-6246?
What are the uses for Vusion?
Which are Vusion UNII Codes?
The UNII codes for the active ingredients in this product are:
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Vusion 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- GLYCOL STEARATE (UNII: 0324G66D0E)
What is the NDC to RxNorm Crosswalk for Vusion?
- RxCUI: 831391 - miconazole nitrate 0.25 % / zinc oxide 15 % / petrolatum 81.4 % Topical Ointment
- RxCUI: 831391 - miconazole nitrate 0.0025 MG/MG / petrolatum 0.814 MG/MG / zinc oxide 0.15 MG/MG Topical Ointment
- RxCUI: 831391 - Miconazole Nitrate 0.0025 MG/MG / Petrolatum 0.814 MG/MG / ZNO 0.15 MG/MG Topical Ointment
- RxCUI: 831391 - miconazole nitrate 0.25 % / petrolatum, white 81.35 % / zinc oxide 15 % Topical Ointment
- RxCUI: 831393 - Vusion 0.25 % / 15 % / 81.35 % Topical 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".