NDC 70945-100 Tolcylen Antifungal Solution
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What is NDC 70945-100?
What are the uses for Tolcylen Antifungal Solution?
Which are Tolcylen Antifungal Solution UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Tolcylen Antifungal Solution 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:
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LACTIC ACID (UNII: 33X04XA5AT)
- ETHYL ACETATE (UNII: 76845O8NMZ)
- UREA (UNII: 8W8T17847W)
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- JOJOBA OIL (UNII: 724GKU717M)
What is the NDC to RxNorm Crosswalk for Tolcylen Antifungal Solution?
- RxCUI: 1988416 - Tolcylen 1 % Topical Solution
- RxCUI: 1988416 - tolnaftate 10 MG/ML Topical Solution [Tolcylen]
- RxCUI: 1988416 - Tolcylen 10 MG/ML Topical Solution
- RxCUI: 313423 - tolnaftate 1 % Topical Solution
- RxCUI: 313423 - tolnaftate 10 MG/ML Topical Solution
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Patient Education
Tolnaftate
Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".