NDC 81877-520 Mometacure
Mometasone Furoate,Dimethicone Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 81877-520?
What are the uses for Mometacure?
Which are Mometacure UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOMETASONE FUROATE (UNII: 04201GDN4R)
- MOMETASONE (UNII: 8HR4QJ6DW8) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Mometacure 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:
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PROPYLENE GLYCOL MONOSTEARATE (UNII: MZM1I680W0)
- PETROLATUM (UNII: 4T6H12BN9U)
- WHITE WAX (UNII: 7G1J5DA97F)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Mometacure?
- RxCUI: 259090 - dimethicone 5 % Topical Cream
- RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
- RxCUI: 311753 - mometasone furoate 0.1 % Topical Cream
- RxCUI: 311753 - mometasone furoate 1 MG/ML Topical Cream
* 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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".