NDC 50090-0524 Major Clotrimazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0524 - Major Clotrimazole
Product Packages
NDC Code 50090-0524-0
Package Description: 1 TUBE in 1 CARTON / 14.17 g in 1 TUBE
Product Details
What is NDC 50090-0524?
What are the uses for Major Clotrimazole?
Which are Major Clotrimazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are Major Clotrimazole 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
What is the NDC to RxNorm Crosswalk for Major Clotrimazole?
- RxCUI: 309367 - clotrimazole 1 % Topical Cream
- RxCUI: 309367 - clotrimazole 10 MG/ML Topical Cream
* Please review the disclaimer below.
Patient Education
Clotrimazole Topical
Topical clotrimazole is used to treat tinea corporis (ringworm; fungal skin infection that causes a red scaly rash on different parts of the body), tinea cruris (jock itch; fungal infection of the skin in the groin or buttocks), and tinea pedis (athlete's foot; fungal infection of the skin on the feet and between the toes). Clotrimazole is in a class of antifungal medications called imidazoles. It works by stopping the growth of fungi that cause infection.
[Learn More]
* 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".