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  4. NDC Product Code: 86994-007 Laramed Antibacterial Alcohol Wipes

NDC 86994-007 Laramed Antibacterial Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 86994-007?
  4. Laramed Antibacterial Alcohol Wipes Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
86994-007
Proprietary Name:
Laramed Antibacterial Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lara Kozmetik Hijyenik Urunleri Sanayi Ve Dis Ticaret Anonim Sirketi
Labeler Code:
86994
Product Label ID:
b0d7b456-7550-a11f-e053-2a95a90a866a
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 86994-007?

The NDC code 86994-007 is assigned by the FDA to the product Laramed Antibacterial Alcohol Wipes which is product labeled by Lara Kozmetik Hijyenik Urunleri Sanayi Ve Dis Ticaret Anonim Sirketi. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 86994-007-18 200 patch in 1 package / 648.8 g in 1 patch (86994-007-17), 86994-007-20 150 patch in 1 package / 486.6 g in 1 patch (86994-007-19), 86994-007-22 120 patch in 1 package / 389.28 g in 1 patch (86994-007-21), 86994-007-24 100 patch in 1 package / 324.4 g in 1 patch (86994-007-23), 86994-007-26 70 patch in 1 package / 227.08 g in 1 patch (86994-007-25), 86994-007-28 50 patch in 1 package / 162.2 g in 1 patch (86994-007-27), 86994-007-30 15 patch in 1 package / 48.66 g in 1 patch (86994-007-29), 86994-007-32 1 patch in 1 package / 3.244 g in 1 patch (86994-007-31). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Laramed Antibacterial Alcohol Wipes?

Open package, removeonewetwipetocleanyourhands| and body. Reseal, keep closed to prevent evaporation. Allow to dry without wiping. Discard properly after use.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Laramed Antibacterial Alcohol Wipes UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Laramed Antibacterial Alcohol 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:

What is the NDC to RxNorm Crosswalk for Laramed Antibacterial Alcohol Wipes?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2398387 - benzalkonium chloride 0.05 % / ethanol 65 % / isopropyl alcohol 10 % Medicated Pad
  • RxCUI: 2398387 - benzalkonium chloride 0.5 MG/ML / ethanol 0.65 ML/ML / isopropyl alcohol 0.1 ML/ML Medicated Pad

* Please review the disclaimer below.

Product Footnotes

[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".