NDC 42593-002 Barielle Fungus Rx Maximum Strength Anti-fungal
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42593-002?
What are the uses for Barielle Fungus Rx Maximum Strength Anti-fungal?
Which are Barielle Fungus Rx Maximum Strength Anti-fungal UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Barielle Fungus Rx Maximum Strength Anti-fungal 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 Fungus Rx Maximum Strength Anti-fungal?
- 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".