NDC 59088-210 Urea 39.5% With 2% Salicylic Acid
Urea,Salicylic Acid Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59088-210?
What are the uses for Urea 39.5% With 2% Salicylic Acid?
What are Urea 39.5% With 2% Salicylic Acid Active Ingredients?
- SALICYLIC ACID 2 g/100g - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
- UREA 39.5 g/100g - A compound formed in the liver from ammonia produced by the deamination of amino acids. It is the principal end product of protein catabolism and constitutes about one half of the total urinary solids.
Which are Urea 39.5% With 2% Salicylic Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- UREA (UNII: 8W8T17847W)
- UREA (UNII: 8W8T17847W) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Urea 39.5% With 2% Salicylic Acid 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SHEA BUTTER (UNII: K49155WL9Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
What is the NDC to RxNorm Crosswalk for Urea 39.5% With 2% Salicylic Acid?
- RxCUI: 2632843 - salicylic acid 2 % / urea 39.5 % Topical Cream
- RxCUI: 2632843 - salicylic acid 20 MG/ML / urea 395 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[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".