NDC 75990-793 Purgo Satin Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75990 - Certus Medical, Inc.
- 75990-793 - Purgo Satin Foam
Product Packages
NDC Code 75990-793-06
Package Description: 1 BAG in 1 BOX / 800 mL in 1 BAG
NDC Code 75990-793-08
Package Description: 1 BAG in 1 BOX / 1000 mL in 1 BAG
Product Details
What is NDC 75990-793?
What are the uses for Purgo Satin Foam?
Which are Purgo Satin Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Purgo Satin Foam 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- LAURIC ACID (UNII: 1160N9NU9U)
- MONOETHANOLAMINE (UNII: 5KV86114PT)
- LACTIC ACID (UNII: 33X04XA5AT)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)
What is the NDC to RxNorm Crosswalk for Purgo Satin Foam?
- RxCUI: 260054 - triclosan 0.3 % Medicated Liquid Soap
- RxCUI: 260054 - triclosan 3 MG/ML Medicated Liquid Soap
- RxCUI: 260054 - triclosan 0.3 % Foaming Medicated Hand Soap
* 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".