NDC 59088-893 Dermacinrx Therazole Pak
Clotrimazole And Betamethasone Dipropionate,Zinc Oxide Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59088-893?
What are the uses for Dermacinrx Therazole Pak?
Which are Dermacinrx Therazole Pak 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Dermacinrx Therazole Pak 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:
- CETEARETH-30 (UNII: 1R9DCZ5FOX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GINGER OIL (UNII: SAS9Z1SVUK)
What is the NDC to RxNorm Crosswalk for Dermacinrx Therazole Pak?
- 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
- RxCUI: 416684 - zinc oxide 20 % Topical Paste
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".