NDC 53603-4002 Antibacterial Mini Wipes Candy Apple
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53603 - Bb17, Llc
- 53603-4002 - Antibacterial Mini Wipes Candy Apple
Product Packages
NDC Code 53603-4002-1
Package Description: .11 g in 1 BAG
Product Details
What is NDC 53603-4002?
What are the uses for Antibacterial Mini Wipes Candy Apple?
Which are Antibacterial Mini Wipes Candy Apple UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Antibacterial Mini Wipes Candy Apple 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)
- ALOE (UNII: V5VD430YW9)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Antibacterial Mini Wipes Candy Apple?
- RxCUI: 1043330 - benzethonium Cl 0.2 % Medicated Pad
- RxCUI: 1043330 - benzethonium chloride 2 MG/ML Medicated Pad
- RxCUI: 1043330 - benzethonium chloride 0.2 % Medicated Wipe
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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".