NDC 86818-005 Neutrevo Alcohol Wet Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 86818 - Sck Zeta Dis Ticaret
- 86818-005 - Neutrevo Alcohol Wet Wipes
Product Packages
NDC Code 86818-005-02
Package Description: 120 PATCH in 1 PACKAGE / 3.04 mL in 1 PATCH (86818-005-01)
NDC Code 86818-005-04
Package Description: 100 PATCH in 1 PACKAGE / 3.04 mL in 1 PATCH (86818-005-03)
NDC Code 86818-005-06
Package Description: 80 PATCH in 1 PACKAGE / 3.04 mL in 1 PATCH (86818-005-05)
Product Details
What is NDC 86818-005?
What are the uses for Neutrevo Alcohol Wet Wipes?
Which are Neutrevo Alcohol Wet Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Neutrevo Alcohol 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Neutrevo Alcohol Wet Wipes?
- RxCUI: 2397698 - ethanol 70 % / hydrogen peroxide 0.125 % Medicated Pad
- RxCUI: 2397698 - ethanol 0.7 ML/ML / hydrogen peroxide 1.25 MG/ML 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".