NDC 50090-3128 Tretinoin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3128 - Tretinoin
Product Packages
NDC Code 50090-3128-0
Package Description: 1 TUBE in 1 CARTON / 20 g in 1 TUBE
Product Details
What is NDC 50090-3128?
What are the uses for Tretinoin?
Which are Tretinoin UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRETINOIN (UNII: 5688UTC01R)
- TRETINOIN (UNII: 5688UTC01R) (Active Moiety)
Which are Tretinoin 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:
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SORBIC ACID (UNII: X045WJ989B)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Tretinoin?
- RxCUI: 106302 - tretinoin 0.025 % Topical Cream
- RxCUI: 106302 - tretinoin 0.25 MG/ML Topical Cream
- RxCUI: 106303 - tretinoin 0.05 % Topical Cream
- RxCUI: 106303 - tretinoin 0.5 MG/ML Topical Cream
- RxCUI: 198300 - tretinoin 0.1 % Topical Cream
* Please review the disclaimer below.
Patient Education
Tretinoin Topical
Tretinoin (Altreno, Atralin, Avita, Retin-A) is used to treat acne. Tretinoin is also used to reduce fine wrinkles (Refissa and Renova) and to improve spotty discoloration (Renova) and rough feeling skin (Renova) when used along with other skin care and sunlight avoidance programs. Tretinoin is in a class of medications called retinoids. It works by promoting peeling of affected skin areas and unclogging pores.
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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".