NDC 68071-4800 Clotrimazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4800 - Clotrimazole
Product Packages
NDC Code 68071-4800-4
Package Description: 45 g in 1 BOX
Product Details
What is NDC 68071-4800?
What are the uses for Clotrimazole?
Which are Clotrimazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
Which are 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- WATER (UNII: 059QF0KO0R)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
What is the NDC to RxNorm Crosswalk for Clotrimazole?
- RxCUI: 309368 - clotrimazole 1 % Vaginal Cream
- RxCUI: 309368 - clotrimazole 10 MG/ML Vaginal Cream
* Please review the disclaimer below.
Patient Education
Clotrimazole Vaginal
Vaginal clotrimazole is used to treat vaginal yeast infections in adults and children 12 years of age and older.. 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".