NDC 90107-3621 After Bite Wipe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 90107 - Adventure Ready Brands
- 90107-3621 - After Bite Wipe
Product Packages
NDC Code 90107-3621-0
Package Description: 1.1 mL in 1 POUCH
NDC Code 90107-3621-1
Package Description: 4 POUCH in 1 BOX / 1.1 mL in 1 POUCH
Product Details
What is NDC 90107-3621?
What are the uses for After Bite Wipe?
Which are After Bite Wipe UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are After Bite Wipe 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:
- MENTHOL (UNII: L7T10EIP3A)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for After Bite Wipe?
- RxCUI: 1190560 - ethanol 50 % / lidocaine HCl 2 % Medicated Pad
- RxCUI: 1190560 - ethanol 0.5 ML/ML / lidocaine hydrochloride 20 MG/ML Medicated Pad
- RxCUI: 1190560 - ethanol 50 % / lidocaine hydrochloride 2 % 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".