NDC 42479-212 Footlogix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42479 - Kvg Group Inc
- 42479-212 - Footlogix
Product Packages
NDC Code 42479-212-17
Package Description: 50 mL in 1 CAN
Product Details
What is NDC 42479-212?
What are the uses for Footlogix?
Which are Footlogix UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are Footlogix 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:
- BUTANE (UNII: 6LV4FOR43R)
- PANTHENOL (UNII: WV9CM0O67Z)
- PROPANE (UNII: T75W9911L6)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AVOCADO (UNII: SDS87L369F)
What is the NDC to RxNorm Crosswalk for Footlogix?
- RxCUI: 358371 - clotrimazole 1 % Topical Spray
- RxCUI: 358371 - clotrimazole 10 MG/ML Topical Spray
* 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".