NDC 51350-011 Curacaine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51350 - Transdermal Corp
- 51350-011 - Curacaine
Product Packages
NDC Code 51350-011-51
Package Description: 1 TUBE in 1 BOX / 30 mL in 1 TUBE (51350-011-01)
Product Details
What is NDC 51350-011?
What are the uses for Curacaine?
Which are Curacaine UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Curacaine 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:
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- WATER (UNII: 059QF0KO0R)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- JOJOBA OIL (UNII: 724GKU717M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Curacaine?
- RxCUI: 1421893 - lidocaine 4 % Topical Cream
- RxCUI: 1421893 - lidocaine 40 MG/ML Topical Cream
* 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".