Lactone Hand Sanitizer Wipe
Product Images NDC 75348-888

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lactone Hand Sanitizer Wipe (NDC 75348-888). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by All One Kozmetik Sanayi Dis Ticaret Anonim Sirketi, 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

Puch (A74550d3 Faef 0f2b E053 2995a90a6b2a)

LACTONE Hand Sanitizer Wipe packaging, featuring a predominantly white and blue design with green accents. The front highlights the product name, hand sanitizer wipe designation, 80% alcohol content, and aloe vera fragrance. The back includes drug facts detailing 80% ethyl alcohol as the active ingredient and various usage and warning instructions. The net weight is 5 grams, and the labeler is ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI, made in Turkey.*

FDA Label Image

A85ee596 6330 5500 E053 2a95a90a715d

LACTONE Hand Sanitizer Wipe packaging label showing front and back views. The front highlights the product name, 80% alcohol content, and aloe vera fragrance. The back includes drug facts with active ingredient ethyl alcohol 80%, warnings, directions, inactive ingredients, and manufacturer information from ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI. Net weight is 5 grams.*

FDA Label Image

Package (Download)

LACTONE Hand Sanitizer Wipe packaging and individual wipe sachet are shown. The box contains 40 wipes and highlights 80% alcohol content with aloe vera fragrance. The packaging states the wipes kill 99.99% of E. coli, Salmonella enterica, and MRSA (Staphylococcus aureus). The labeler is ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI.*

* 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.