NDC 68927-3492 Fungazoil Advanced
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68927 - Pedifix
- 68927-3492 - Fungazoil Advanced
Product Packages
NDC Code 68927-3492-1
Package Description: 15 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 68927-3492?
What are the uses for Fungazoil Advanced?
Which are Fungazoil Advanced UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are Fungazoil Advanced 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:
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- WATER (UNII: 059QF0KO0R)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- EMU OIL (UNII: 344821WD61)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- SOYBEAN OIL (UNII: 241ATL177A)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- TEA TREE OIL (UNII: VIF565UC2G)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- JOJOBA OIL (UNII: 724GKU717M)
- UREA (UNII: 8W8T17847W)
What is the NDC to RxNorm Crosswalk for Fungazoil Advanced?
- RxCUI: 1540223 - FungaZoil 1 % Topical Solution
- RxCUI: 1540223 - clotrimazole 10 MG/ML Topical Solution [Fungazoil]
- RxCUI: 1540223 - Fungazoil 1 % Topical Solution
- RxCUI: 1540223 - Fungazoil 10 MG/ML Topical Solution
- RxCUI: 309370 - clotrimazole 1 % 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".