NDC 70242-104 Fungisolve Tolnaftate Antifungal
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What is NDC 70242-104?
What are the uses for Fungisolve Tolnaftate Antifungal?
Which are Fungisolve Tolnaftate Antifungal UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Fungisolve Tolnaftate Antifungal 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- WATER (UNII: 059QF0KO0R)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
What is the NDC to RxNorm Crosswalk for Fungisolve Tolnaftate Antifungal?
- RxCUI: 1790296 - FUNGISOLVE 1 % Topical Spray
- RxCUI: 1790296 - tolnaftate 10 MG/ML Topical Spray [Fungisolve]
- RxCUI: 1790296 - Fungisolve 1 % Topical Spray
- RxCUI: 313421 - tolnaftate 1 % Topical Spray
- RxCUI: 313421 - tolnaftate 10 MG/ML Topical Spray
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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".