NDC 72835-502 Elemar Patch
Lidocaine Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 72835-502?
What are the uses for Elemar Patch?
Which are Elemar Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Elemar Patch 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- UREA (UNII: 8W8T17847W)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- KAOLIN (UNII: 24H4NWX5CO)
- TARTARIC ACID (UNII: W4888I119H)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- GRAPEFRUIT SEED OIL (UNII: 598D944HOL)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
- ROSA CENTIFOLIA FLOWER OIL (UNII: H32V31VMWY)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- WITCH HAZEL (UNII: 101I4J0U34)
- YUCCA SCHIDIGERA ROOT (UNII: E2H9ET15AT)
- ORANGE PEEL (UNII: TI9T76XD44)
- LEMON OIL (UNII: I9GRO824LL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
What is the NDC to RxNorm Crosswalk for Elemar Patch?
- RxCUI: 1745091 - lidocaine 5 % Medicated Patch
- RxCUI: 1745091 - lidocaine 0.05 MG/MG Medicated Patch
- RxCUI: 415976 - menthol 6 % Topical Gel
- RxCUI: 415976 - menthol 0.06 MG/MG Topical Gel
* 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".