NDC 59088-731 Xyliderm
Lidocaine,Isopropyl Alcohol Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59088-731?
What are the uses for Xyliderm?
Which are Xyliderm UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Xyliderm 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- UREA (UNII: 8W8T17847W)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- GELATIN (UNII: 2G86QN327L)
- KAOLIN (UNII: 24H4NWX5CO)
- TARTARIC ACID (UNII: W4888I119H)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SORBITOL (UNII: 506T60A25R)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Xyliderm?
- RxCUI: 1745091 - lidocaine 5 % Medicated Patch
- RxCUI: 1745091 - lidocaine 0.05 MG/MG Medicated Patch
- RxCUI: 2642344 - Lidocan 5 % Medicated Patch
- RxCUI: 2642344 - lidocaine 0.05 MG/MG Medicated Patch [Lidocan]
- RxCUI: 2642344 - Lidocan 0.05 MG/MG Medicated Patch
* 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.
[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.
[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".