NDC 55443-0102 Vionex Towelette
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55443 - Metrex Research
- 55443-0102 - Vionex Towelette
Product Packages
NDC Code 55443-0102-3
Package Description: 10 BOX in 1 CASE / 50 PACKET in 1 BOX (55443-0102-2) / 2.7 g in 1 PACKET (55443-0102-1)
Product Details
What is NDC 55443-0102?
What are the uses for Vionex Towelette?
Which are Vionex Towelette UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Vionex Towelette?
- RxCUI: 1044919 - VioNex 0.5 % Medicated Pad
- RxCUI: 1044919 - chloroxylenol 5 MG/ML Medicated Pad [VioNex]
- RxCUI: 1044919 - VioNex 0.5 % Medicated Towelette
- RxCUI: 1044919 - VioNex 5 MG/ML Medicated Pad
- RxCUI: 844372 - chloroxylenol 0.5 % 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".