NDC 61619-717 Antisepation
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61619 - A-cute Derm, Incorporated
- 61619-717 - Antisepation
Product Packages
NDC Code 61619-717-10
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 29.6 mL in 1 BOTTLE, PLASTIC (61619-717-07)
NDC Code 61619-717-12
Package Description: 946.4 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-717-14
Package Description: 118.294 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-717-18
Package Description: 236.6 mL in 1 BOTTLE, PLASTIC
NDC Code 61619-717-28
Package Description: 3800 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 61619-717?
What are the uses for Antisepation?
Which are Antisepation UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Antisepation 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:
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE (UNII: 1EO3O1X7HG)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Antisepation?
- RxCUI: 1243889 - benzethonium chloride 0.2 % Medicated Liquid Soap
- RxCUI: 1243889 - benzethonium 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".