NDC 74146-236 Epic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 74146-236-02
Package Description: 4 CONTAINER in 1 BOX / 3785.41 mL in 1 CONTAINER (74146-236-01)
NDC Code 74146-236-04
Package Description: 4 CONTAINER in 1 BOX / 3785.41 mL in 1 CONTAINER (74146-236-03)
NDC Code 74146-236-05
Package Description: 18927.1 mL in 1 DRUM
NDC Code 74146-236-06
Package Description: 18927.1 mL in 1 DRUM
NDC Code 74146-236-07
Package Description: 208198 mL in 1 DRUM
NDC Code 74146-236-08
Package Description: 208198 mL in 1 DRUM
NDC Code 74146-236-09
Package Description: 113562 mL in 1 DRUM
NDC Code 74146-236-10
Package Description: 113562 mL in 1 DRUM
NDC Code 74146-236-11
Package Description: 56781.2 mL in 1 DRUM
NDC Code 74146-236-12
Package Description: 56781.2 mL in 1 DRUM
NDC Code 74146-236-14
Package Description: 4 JUG in 1 BOX / 3550 mL in 1 JUG (74146-236-13)
NDC Code 74146-236-16
Package Description: 4 JUG in 1 BOX / 3550 mL in 1 JUG (74146-236-15)
NDC Code 74146-236-18
Package Description: 4 JUG in 1 BOX / 2500 mL in 1 JUG (74146-236-17)
NDC Code 74146-236-20
Package Description: 4 JUG in 1 BOX / 2500 mL in 1 JUG (74146-236-19)
Product Details
What is NDC 74146-236?
What are the uses for Epic?
Which are Epic UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Epic 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
What is the NDC to RxNorm Crosswalk for Epic?
- RxCUI: 1233282 - benzalkonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1233282 - benzalkonium chloride 1 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".