NDC 76725-004 Dr.clinic Antibacterial Wet Wipes Alcohol Free
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76725 - Makyaj Kozmetik Insaat Sanayi Ve Ticaret Limited Sirketi
- 76725-004 - Dr.clinic Antibacterial Wet Wipes Alcohol Free
Product Packages
NDC Code 76725-004-01
Package Description: 1 PACKET in 1 PACKAGE / 4.17 g in 1 PACKET
NDC Code 76725-004-02
Package Description: 12 PACKET in 1 PACKAGE / 4.17 g in 1 PACKET
NDC Code 76725-004-03
Package Description: 40 PACKET in 1 PACKAGE / 4.17 g in 1 PACKET
NDC Code 76725-004-04
Package Description: 72 PACKET in 1 PACKAGE / 4.17 g in 1 PACKET
Product Details
What is NDC 76725-004?
What are the uses for Dr.clinic Antibacterial Wet Wipes Alcohol Free?
Which are Dr.clinic Antibacterial Wet Wipes Alcohol Free UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dr.clinic Antibacterial Wet Wipes Alcohol Free 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)
- CORN OIL (UNII: 8470G57WFM)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Dr.clinic Antibacterial Wet Wipes Alcohol Free?
- RxCUI: 2360919 - benzalkonium Cl 0.2 % Medicated Pad
- RxCUI: 2360919 - benzalkonium chloride 2 MG/ML Medicated Pad
- RxCUI: 2360919 - benzalkonium 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".