NDC 59088-801 Lextol
Diclofenac Sodium,Capsaicin Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 59088-801?
What are the uses for Lextol?
Which are Lextol UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
- CAPSICUM OLEORESIN (UNII: UW86K581WY)
- CAPSICUM OLEORESIN (UNII: UW86K581WY) (Active Moiety)
Which are Lextol 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)
- ALCOHOL (UNII: 3K9958V90M)
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- ACAI OIL (UNII: Z0W6766A2W)
- ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)
- HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- STARCH, CORN (UNII: O8232NY3SJ)
- AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)
- LINSEED OIL (UNII: 84XB4DV00W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- CORN SYRUP (UNII: 9G5L16BK6N)
- OCTENYLSUCCINIC ANHYDRIDE (UNII: 4YWS14FAXH)
- LAURYL LAURATE (UNII: GPW77G0937)
- METHACRYLIC ACID-ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)
What is the NDC to RxNorm Crosswalk for Lextol?
- RxCUI: 198555 - capsaicin 0.025 % Topical Cream
- RxCUI: 198555 - capsaicin 0.25 MG/ML Topical Cream
- RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
- RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution
- RxCUI: 857700 - diclofenac sodium 1.5 % (as diclofenac sodium 16.05 MG/ML) Topical Solution
* 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".