NDC 50090-3032 Finacea
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3032 - Finacea
Product Packages
NDC Code 50090-3032-0
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Details
What is NDC 50090-3032?
What are the uses for Finacea?
Which are Finacea UNII Codes?
The UNII codes for the active ingredients in this product are:
- AZELAIC ACID (UNII: F2VW3D43YT)
- AZELAIC ACID (UNII: F2VW3D43YT) (Active Moiety)
Which are Finacea 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:
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- 1,2-DIARACHIDOYL-SN-GLYCERO-3-PHOSPHOCHOLINE (UNII: HE0P2D9ZLS)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Finacea?
- RxCUI: 1041518 - azelaic acid 15 % Topical Gel
- RxCUI: 1041518 - azelaic acid 0.15 MG/MG Topical Gel
- RxCUI: 1043748 - Finacea 15 % Topical Gel
- RxCUI: 1043748 - azelaic acid 0.15 MG/MG Topical Gel [Finacea]
- RxCUI: 1043748 - Finacea 0.15 MG/MG Topical Gel
* Please review the disclaimer below.
Patient Education
Azelaic Acid Topical
Azelaic acid gel and foam is used to clear the bumps, lesions, and swelling caused by rosacea (a skin disease that causes redness, flushing, and pimples on the face). Azelaic acid cream is used to treat the pimples and swelling caused by acne. Azelaic acid is in a class of medications called dicarboxylic acids. It works to treat rosacea by decreasing the swelling and redness of the skin. It works to treat acne by killing the bacteria that infect pores and by decreasing production of keratin, a natural substance that can lead to the development of acne.
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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".