Kai Klean
Product Images NDC 74918-002

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Kai Klean (NDC 74918-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bender Consulting Ltd, 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

1000ml Label (Kai Klean Hand Sanitizer 1000ml 5 6 20)

KAI KLEAN Hand Sanitizer 1000 mL packaging label showing the product name prominently with 80% alcohol antiseptic strength. The label includes usage indications, warnings, directions, and other information, along with inactive ingredients and manufacturer details for Bender Consulting Ltd. The product is a topical, non-sterile hand sanitizer solution.*

FDA Label Image

100 mL Flip Top Label (Kai Klean Hand Sanitizer 100ml Flip Top 5 6 20)

KAI KLEAN Hand Sanitizer 100 mL flip top bottle label by Bender Consulting Ltd. The label highlights 80% alcohol antiseptic strength and identifies the product as a topical, non-sterile solution. The label includes a Drug Facts panel detailing active ingredient alcohol 80% v/v, usage instructions, warnings, directions, storage information, and inactive ingredients. The product is made in Vietnam and packaged for Bender Consulting Ltd, Honolulu, HI.*

FDA Label Image

100 mL Spray Label (Kai Klean Hand Sanitizer 100ml Spray 5 6 20)

KAI KLEAN Hand Sanitizer 100 mL spray bottle label with 80% alcohol antiseptic strength. The label includes the product name in large font, highlighting it as a non-sterile topical solution. The back panel features drug facts with active and inactive ingredients, warnings, directions, storage instructions, and packaging details by Bender Consulting Ltd, Honolulu, HI.*

FDA Label Image

1800ml Label (Kai Klean Hand Sanitizer 1800ml 5 6 20)

KAI KLEAN Hand Sanitizer 1800 mL label shows product name with 80% Alcohol antiseptic concentration. The label states it is a topical, non-sterile solution. Includes a turquoise and blue color scheme with text emphasizing alcohol antiseptic 80%, and a droplet graphic. The labeler is Bender Consulting Ltd.*

FDA Label Image

2000ml Label (Kai Klean Hand Sanitizer 2000ml 5 6 20)

KAI KLEAN Hand Sanitizer 2000 mL label shows an 80% alcohol antiseptic topical, non-sterile solution. The front panel is teal with white and blue text highlighting the product and volume. The back panel contains drug facts including active ingredient alcohol 80% v/v, usage instructions, warnings, directions, storage recommendations, and inactive ingredients. Packaged for Bender Consulting Ltd, Honolulu, HI, product of Vietnam, with a barcode at the bottom.*

FDA Label Image

2700ml Label (Kai Klean Hand Sanitizer 2700ml 5 6 20)

KAI KLEAN Hand Sanitizer 2700 mL label shows the product name with the active ingredient alcohol 80% v/v as an antiseptic. It is labeled as a topical, non-sterile solution. The label includes manufacturer information for Bender Consulting Ltd, Honolulu, HI, and states the product is made in Vietnam. The label features drug facts with directions, warnings, and inactive ingredients.*

FDA Label Image

300ml Label (Kai Klean Hand Sanitizer 300ml 5 6 20)

The image shows the front and back label of KAI KLEAN Hand Sanitizer, a 300 mL topical antiseptic solution. The front highlights 80% alcohol content, non-sterile solution, and antiseptic use. The back panel presents drug facts including active ingredient alcohol 80% v/v, warnings, directions, and storage instructions. The product is labeled by Bender Consulting Ltd and marked as a product of Vietnam.*

* 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.