NDC 50090-1026 Mometasone Furoate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-1026 - Mometasone Furoate
Product Packages
NDC Code 50090-1026-0
Package Description: 15 g in 1 TUBE
Product Details
What is NDC 50090-1026?
What are the uses for Mometasone Furoate?
Which are Mometasone Furoate UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOMETASONE FUROATE (UNII: 04201GDN4R)
- MOMETASONE (UNII: 8HR4QJ6DW8) (Active Moiety)
Which are Mometasone Furoate 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)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PROPYLENE GLYCOL MONOPALMITOSTEARATE (UNII: F76354LMGR)
- WHITE WAX (UNII: 7G1J5DA97F)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Mometasone Furoate?
- RxCUI: 151029 - mometasone furoate 0.1 % Topical Ointment
- RxCUI: 151029 - mometasone furoate 0.001 MG/MG Topical Ointment
- RxCUI: 151029 - mometasone furoate 1 MG/GM Topical Ointment
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Patient Education
Mometasone Topical
Mometasone topical is used to relieve the redness, swelling, itching and inflammation and discomfort of various skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). Mometasone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
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* Please review the disclaimer below.
[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".