Konix
Product Images NDC 73107-102

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Konix (NDC 73107-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image Description (Konix Covid Healthcare 150 mL)

Image Description (Konix Covid Healthcare  150 mL)
KONIX Alcohol Antiseptic 80% Topical Solution Antiseptic Hand Rub in a 150 mL (5 fl. oz.) bottle is labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS. The label highlights its active ingredient as 80% alcohol with antiseptic purpose, warnings, directions, and inactive ingredients including glycerin and hydrogen peroxide.*
FDA Label Image

Image Description (Konix Covid Healthcare 30 mL)

Image Description (Konix Covid Healthcare  30 mL)
KONIX Alcohol Antiseptic 80% Topical Solution Antiseptic Hand Rub in a 30 mL (1 fl. oz.) package by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS. The front label states it is a non-sterile solution. The back label includes Drug Facts with active ingredient 80% alcohol as antiseptic, usage instructions, warnings, storage conditions, and inactive ingredients including glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

Image Description (Konix Covid Healthcare 50 mL)

Image Description (Konix Covid Healthcare  50 mL)
Label for KONIX Alcohol Antiseptic 80% Topical Solution, an antiseptic hand rub in a 50 mL (1.7 fl. oz.) bottle. The label features the KONIX brand name prominently with dosage strength and purpose noted. The product is labeled as a non-sterile solution and is manufactured by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS.*
FDA Label Image

Image Description (Konix Covid Healthcare 500 mL)

Image Description (Konix Covid Healthcare  500 mL)
KONIX Alcohol Antiseptic 80% Topical Solution antiseptic hand rub in a 500 mL (16.9 fl. oz.) container. The label includes the brand name KONIX in a blue geometric design, with the product described as a non-sterile antiseptic hand rub solution. The manufacturer is Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS.*
FDA Label Image

Image Description (Konix Covid Healthcare 5000 mL)

Image Description (Konix Covid Healthcare  5000 mL)
The label for KONIX Alcohol Antiseptic 80% Topical Solution, an antiseptic hand rub provided in a 5000 mL (169 fl oz) volume. The product is labeled as a non-sterile solution by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS. The label includes Drug Facts detailing the active ingredient (80% alcohol), purpose (antiseptic), warnings, directions, and inactive ingredients (glycerin, hydrogen peroxide, purified water USP).*
FDA Label Image

Image Description (Konix Covid Healthcare 100 mL)

Image Description (Konix Covid Healthcare 100 mL)
KONIX Alcohol Antiseptic 80% Topical Solution Antiseptic Hand Rub in a 100 mL (3.4 fl. oz.) container. The label indicates it is a non-sterile solution manufactured by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS. The product is identified by the NDC 73107-102.*
FDA Label Image

Image Description (Konix Covid Healthcare 1000 mL)

Image Description (Konix Covid Healthcare 1000 mL)
KONIX Alcohol Antiseptic 80% Topical Solution hand rub in a 1000 mL (33.8 fl. oz.) bottle. The label states it is an antiseptic hand rub and non-sterile solution. It is manufactured by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS. The label details active ingredient, alcohol 80% v/v, purpose as antiseptic, directions for use, warnings, and inactive ingredients including glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

Image Description (Konix Covid Healthcare 200 mL)

Image Description (Konix Covid Healthcare 200 mL)
KONIX Alcohol Antiseptic 80% Topical Solution 200 mL (6.7 fl. oz.) antiseptic hand rub in a non-sterile solution. The label features the brand KONIX prominently with product details including volume and antiseptic strength. It is manufactured by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS with the NDC 73107-102.*
FDA Label Image

Image Description (Konix Covid Healthcare 250 mL)

Image Description (Konix Covid Healthcare 250 mL)
Label for KONIX Alcohol Antiseptic 80% Topical Solution, an antiseptic hand rub in a 250 mL (8.5 fl. oz.) non-sterile liquid form. The label indicates the active ingredient is 80% alcohol. Manufacturer is Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS. The label includes usage instructions, warnings, directions, and inactive ingredients listed on the adjacent drug facts panel.*
FDA Label Image

Image Description (Konix Covid Healthcare 85 mL)

Image Description (Konix Covid Healthcare 85 mL)
Label for KONIX Alcohol Antiseptic 80% Topical Solution, an antiseptic hand rub in a non-sterile solution form. The container holds 85 mL (2.8 fl. oz.). The label displays the product's active ingredient alcohol 80% v/v and includes manufacturer information for Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS.*
FDA Label Image

Image Description (Covid Packet 5ml)

Image Description (Covid Packet  5ml)
KONIX Alcohol Antiseptic 80% Antiseptic Hand Rub topical solution in a 5 mL non-sterile package. The label includes a blue geometric design with the KONIX logo and dosage details. It is labeled by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi ve Tic. AS with NDC 73107-102.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.