NDC 50672-838 Antibacterial Wet Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 50672-838?
What are the uses for Antibacterial Wet Wipes?
Which are Antibacterial Wet Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Wet Wipes 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)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- GLYCERIN (UNII: PDC6A3C0OX)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- TOCOPHERYL NICOTINATE, D-.ALPHA. (UNII: WI1J5UCY5C)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALLANTOIN (UNII: 344S277G0Z)
What is the NDC to RxNorm Crosswalk for Antibacterial Wet Wipes?
- RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
* 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".