NDC 65734-270 Antiseptic Formula Filled Swab
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65734 - Swabplus Inc.
- 65734-270 - Antiseptic Formula Filled Swab
Product Characteristics
Product Packages
NDC Code 65734-270-72
Package Description: 72 APPLICATOR in 1 PACKET / .15 mL in 1 APPLICATOR (65734-270-00)
Product Details
What is NDC 65734-270?
What are the uses for Antiseptic Formula Filled Swab?
Which are Antiseptic Formula Filled Swab UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antiseptic Formula Filled Swab 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)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Antiseptic Formula Filled Swab?
- RxCUI: 1374383 - benzalkonium Cl 0.11 % / lidocaine HCl 1 % Medicated Pad
- RxCUI: 1374383 - benzalkonium chloride 1.1 MG/ML / lidocaine hydrochloride 10 MG/ML Medicated Pad
- RxCUI: 1374383 - benzalkonium chloride 0.11 % / lidocaine hydrochloride 1 % Medicated Pad
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[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".