NDC 70786-0258 Clotrimazole And Betamethasone Dipropionate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70786 - Unit Dose Services
- 70786-0258 - Clotrimazole And Betamethasone Dipropionate
Product Packages
NDC Code 70786-0258-1
Package Description: 15 g in 1 TUBE
Product Details
What is NDC 70786-0258?
What are the uses for Clotrimazole And Betamethasone Dipropionate?
Which are Clotrimazole And Betamethasone Dipropionate 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)
Which are Clotrimazole And Betamethasone Dipropionate 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARETH-30 (UNII: 1R9DCZ5FOX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
What is the NDC to RxNorm Crosswalk for Clotrimazole And Betamethasone Dipropionate?
- 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".