NDC 55992-717 Nail Md
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What is NDC 55992-717?
What are the uses for Nail Md?
Which are Nail Md UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Nail Md 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:
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- FUSIDIC ACID (UNII: 59XE10C19C)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for Nail Md?
- RxCUI: 1486762 - tolnaftate 1 % / triclosan 0.2 % Topical Spray
- RxCUI: 1486762 - tolnaftate 10 MG/ML / triclosan 2 MG/ML Topical Spray
- RxCUI: 1486762 - Tolnaftate 1 % / Triclosan 0.2 % Topical Spray
- RxCUI: 1486787 - Nail MD 0.2 % / 1 % Topical Spray
- RxCUI: 1486787 - tolnaftate 10 MG/ML / triclosan 2 MG/ML Topical Spray [Nail MD 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".