NDC 52261-0502 Forticept Antifungal Cooling
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52261 - Cosco International, Inc.
- 52261-0502 - Forticept Antifungal Cooling
Product Packages
NDC Code 52261-0502-0
Package Description: 60 g in 1 BOTTLE, SPRAY
NDC Code 52261-0502-1
Package Description: 120 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 52261-0502?
What are the uses for Forticept Antifungal Cooling?
Which are Forticept Antifungal Cooling UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are Forticept Antifungal Cooling 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- OAT (UNII: Z6J799EAJK)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- TEA TREE OIL (UNII: VIF565UC2G)
What is the NDC to RxNorm Crosswalk for Forticept Antifungal Cooling?
- RxCUI: 309370 - clotrimazole 1 % Topical Solution
- RxCUI: 309370 - clotrimazole 10 MG/ML Topical Solution
* Please review the disclaimer below.
[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".