NDC 59088-391 Dermacinrx Clorhexacin
Mupirocin Ointment Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59088-391?
What are the uses for Dermacinrx Clorhexacin?
Which are Dermacinrx Clorhexacin UNII Codes?
The UNII codes for the active ingredients in this product are:
- MUPIROCIN (UNII: D0GX863OA5)
- MUPIROCIN (UNII: D0GX863OA5) (Active Moiety)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- CHLORHEXIDINE (UNII: R4KO0DY52L) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Dermacinrx Clorhexacin 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:
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- WATER (UNII: 059QF0KO0R)
- TRIDECYL ALCOHOL (UNII: 8I9428H868)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LEVOMENOL (UNII: 24WE03BX2T)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- GINGER (UNII: C5529G5JPQ)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Dermacinrx Clorhexacin?
- RxCUI: 106346 - mupirocin 2 % Topical Ointment
- RxCUI: 106346 - mupirocin 0.02 MG/MG Topical Ointment
- RxCUI: 106346 - mupirocin 20 MG per GM Topical Ointment
- RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Liquid Soap
- RxCUI: 211365 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap
* 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".