NDC 81959-0001 Pantin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81959 - Tmt America Llc
- 81959-0001 - Pantin
Product Packages
NDC Code 81959-0001-1
Package Description: 1 JAR in 1 CARTON / 100 g in 1 JAR
NDC Code 81959-0001-3
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 30 g in 1 TUBE, WITH APPLICATOR
NDC Code 81959-0001-5
Package Description: 1 JAR in 1 CARTON / 50 g in 1 JAR
Product Details
What is NDC 81959-0001?
What are the uses for Pantin?
Which are Pantin UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Pantin 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:
- PARAFFIN (UNII: I9O0E3H2ZE)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
- LIQUID PETROLEUM (UNII: 6ZAE7X688J)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Pantin?
- RxCUI: 1534792 - lidocaine 5 % Topical Cream
- RxCUI: 1534792 - lidocaine 50 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".