NDC 71589-009 Desonide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71589 - Aleor Dermaceuticals Limited
- 71589-009 - Desonide
Product Packages
NDC Code 71589-009-18
Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
NDC Code 71589-009-59
Package Description: 1 BOTTLE in 1 CARTON / 59 mL in 1 BOTTLE
Product Details
What is NDC 71589-009?
What are the uses for Desonide?
Which are Desonide UNII Codes?
The UNII codes for the active ingredients in this product are:
- DESONIDE (UNII: J280872D1O)
- DESONIDE (UNII: J280872D1O) (Active Moiety)
Which are Desonide 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Desonide?
- RxCUI: 197572 - desonide 0.05 % Topical Lotion
- RxCUI: 197572 - desonide 0.5 MG/ML Topical Lotion
* Please review the disclaimer below.
Patient Education
Desonide Topical
Desonide is used to treat the redness, swelling, itching, 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). Desonide is in a class of medications called topical 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".