NDC 90025-079 Scrub-a-dub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 90025 - Titan Industrial Chemicals, Llc
- 90025-079 - Scrub-a-dub
Product Packages
NDC Code 90025-079-04
Package Description: 4 BOTTLE, PLASTIC in 1 BOX / 3784 g in 1 BOTTLE, PLASTIC (90025-079-01)
Product Details
What is NDC 90025-079?
What are the uses for Scrub-a-dub?
Which are Scrub-a-dub UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Scrub-a-dub 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:
- HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) (UNII: X70SE62ZAR)
- COCO-BETAINE (UNII: 03DH2IZ3FY)
- COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)
- WATER (UNII: 059QF0KO0R)
- LEMON OIL (UNII: I9GRO824LL)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Scrub-a-dub?
- RxCUI: 1439778 - benzalkonium chloride 0.2 % Medicated Liquid Soap
- RxCUI: 1439778 - benzalkonium chloride 2 MG/ML Medicated Liquid 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".