NDC 73575-010 Pliaglis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73575 - Oba Pharmaceuticals, Inc.
- 73575-010 - Pliaglis
Product Packages
NDC Code 73575-010-02
Package Description: 2 TUBE in 1 CARTON / 30 g in 1 TUBE
NDC Code 73575-010-04
Package Description: 4 TUBE in 1 CARTON / 30 g in 1 TUBE
NDC Code 73575-010-09
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
Product Details
What is NDC 73575-010?
What are the uses for Pliaglis?
Which are Pliaglis UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- TETRACAINE (UNII: 0619F35CGV)
- TETRACAINE (UNII: 0619F35CGV) (Active Moiety)
Which are Pliaglis 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
What is the NDC to RxNorm Crosswalk for Pliaglis?
- RxCUI: 687443 - lidocaine 7 % / tetracaine 7 % Topical Cream
- RxCUI: 687443 - lidocaine 70 MG/ML / tetracaine 70 MG/ML Topical Cream
- RxCUI: 728126 - Pliaglis (lidocaine 7 % / tetracaine 7 % ) Topical Cream
- RxCUI: 728126 - lidocaine 70 MG/ML / tetracaine 70 MG/ML Topical Cream [Pliaglis]
* 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".