NDC 73519-003 Clotrimazol
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 73519-003?
Which are Clotrimazol UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are Clotrimazol 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:
- PEG-20 SORBITAN STEARATE (UNII: HD40WR33LC)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PEG-25 PROPYLENE GLYCOL STEARATE (UNII: X21KPH4633)
- WATER (UNII: 059QF0KO0R)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
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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".