NDC 42593-001 Barielle Professional Maximum Strength Fungus Rx Antifungal Pro
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42593-001?
What are the uses for Barielle Professional Maximum Strength Fungus Rx Antifungal Pro?
Which are Barielle Professional Maximum Strength Fungus Rx Antifungal Pro UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Barielle Professional Maximum Strength Fungus Rx Antifungal Pro 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:
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-20 (UNII: I835H2IHHX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- OCTOXYNOL 9 (UNII: 7JPC6Y25QS)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- IMIDUREA (UNII: M629807ATL)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Barielle Professional Maximum Strength Fungus Rx Antifungal Pro?
- RxCUI: 1243478 - FungusRx 1 % Topical Solution
- RxCUI: 1243478 - tolnaftate 10 MG/ML Topical Solution [FungusRx]
- RxCUI: 1243478 - FungusRx 10 MG/ML Topical Solution
- RxCUI: 313423 - tolnaftate 1 % Topical Solution
- RxCUI: 313423 - tolnaftate 10 MG/ML Topical Solution
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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".