NDC 86994-008 Laramed Antibacterial Hand Sanitizer Gel

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
86994-008
Proprietary Name:
Laramed Antibacterial Hand Sanitizer Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
86994
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 86994-008?

The NDC code 86994-008 is assigned by the FDA to the product Laramed Antibacterial Hand Sanitizer Gel 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 14 packages with assigned NDC codes 86994-008-01 5000 ml in 1 bottle, plastic , 86994-008-02 10000 ml in 1 bottle, plastic , 86994-008-03 50000 ml in 1 bottle, plastic , 86994-008-04 1000 ml in 1 bottle, plastic , 86994-008-06 750 ml in 1 bottle, plastic , 86994-008-07 500 ml in 1 bottle, plastic , 86994-008-08 400 ml in 1 bottle, plastic , 86994-008-09 300 ml in 1 bottle, plastic , 86994-008-13 100 ml in 1 bottle, plastic , 86994-008-15 50 ml in 1 bottle, plastic , 86994-008-16 150 ml in 1 bottle, plastic , 86994-008-17 200 ml in 1 bottle, plastic , 86994-008-18 250 ml in 1 bottle, plastic , 86994-008-19 800 ml in 1 bottle, plastic . 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 Hand Sanitizer Gel?

Place enough product in your palm to cover hands and rub hands together briskly until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

What is the NDC to RxNorm Crosswalk for Laramed Antibacterial Hand Sanitizer Gel?

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: 2397131 - ethanol 70 % / isopropyl alcohol 10 % Topical Gel
  • RxCUI: 2397131 - ethanol 0.7 ML/ML / isopropyl alcohol 0.1 ML/ML Topical Gel

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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".