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  4. NDC Product Code: 86994-006 Lara Med Antibacterial Hand Skin Cleaner

NDC 86994-006 Lara Med Antibacterial Hand Skin Cleaner

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 86994-006?
  4. Lara Med Antibacterial Hand Skin Cleaner Uses
  5. 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:
86994-006
Proprietary Name:
Lara Med Antibacterial Hand Skin Cleaner
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:
ab72a082-e299-baf4-e053-2a95a90a6a89
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 86994-006?

The NDC code 86994-006 is assigned by the FDA to the product Lara Med Antibacterial Hand Skin Cleaner 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 3 packages with assigned NDC codes 86994-006-01 100 ml in 1 bottle, spray , 86994-006-02 150 ml in 1 bottle, spray , 86994-006-03 300 ml in 1 bottle, spray . 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 Lara Med Antibacterial Hand Skin Cleaner?

Use 3 ml product in your palm and hands. Rubbed well for 30 seconds. Allow to dry without wiping. Discard properly after use.Supervise children under 6 years of age when using this product to avoid swallowing.

What is the NDC to RxNorm Crosswalk for Lara Med Antibacterial Hand Skin Cleaner?

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: 2397709 - ethanol 60.7 % / isopropyl alcohol 8.7 % Topical Spray
  • RxCUI: 2397709 - ethanol 0.607 ML/ML / isopropyl alcohol 0.087 ML/ML Topical Spray

* 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".