NDC 16590-033 Betamethasone Clotrimazole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa
- 16590-033 - Betamethasone Clotrimazole
Product Packages
NDC Code 16590-033-15
Package Description: 1 CREAM in 1 CARTON
Product Details
What is NDC 16590-033?
What are the uses for Betamethasone Clotrimazole?
Which are Betamethasone Clotrimazole UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOTRIMAZOLE (UNII: G07GZ97H65)
- CLOTRIMAZOLE (UNII: G07GZ97H65) (Active Moiety)
- BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U)
- BETAMETHASONE (UNII: 9842X06Q6M) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Betamethasone Clotrimazole?
- RxCUI: 308714 - clotrimazole 1 % / betamethasone 0.05 % Topical Cream
- RxCUI: 308714 - betamethasone 0.5 MG/ML / clotrimazole 10 MG/ML Topical Cream
- RxCUI: 308714 - betamethasone 0.05 % / clotrimazole 1 % Topical Cream
- RxCUI: 308714 - betamethasone 0.5 MG/ML (betamethasone dipropionate 0.64 MG/ML) / clotrimazole 10 MG/ML Topical Cream
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[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".