NDC 55992-711 Nail Md
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Product Details
What is NDC 55992-711?
What are the uses for Nail Md?
Which are Nail Md UNII Codes?
The UNII codes for the active ingredients in this product are:
- MICONAZOLE NITRATE (UNII: VW4H1CYW1K)
- MICONAZOLE (UNII: 7NNO0D7S5M) (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:
- BIOTIN (UNII: 6SO6U10H04)
- WATER (UNII: 059QF0KO0R)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- BIS-ETHOXYDIGLYCOL SUCCINATE (UNII: YGQ120RH3I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALCOHOL (UNII: 3K9958V90M)
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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".