Creamol Hand Sanitizer Wipe
Product Images NDC 77892-0009

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Creamol Hand Sanitizer Wipe (NDC 77892-0009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laber Kimya Ar-ge Sanayi Ticaret - Levent Kahriman, 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

Ndc: 77892-0009-1 Inner (Label Back)

Drug Facts panel for Creamol Hand Sanitizer Wipe lists ethanol alcohol 80% as the active antimicrobial ingredient. It provides directions for use as a hand sanitizer to help reduce bacteria and warnings about flammability, external use only, eye contact, and keeping out of reach of children. Additional information includes potential discoloration of fabrics and the manufacturer's address in Turkey. It states the product is not for individual sale and includes importer information.*

FDA Label Image

Ndc: 77892-0009-1 Inner (Label)

Creamol Hand Sanitizer Wipe packaging label features a blue and white color scheme with the brand name Creamol prominently displayed at the top. The label highlights that it is a hand sanitizing wipe that kills 99.9% of most common germs, is gentle on hands, and contains an alcohol formula. The labeler is LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN.*

FDA Label Image

Ndc: 77892-0009-1 Outer (Outer Package)

Packaging label for Creamol Hand Sanitizer Wipe by LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN. The label highlights the product as hand sanitizing wipes with a blue gradient background, featuring individual wipe packets and emphasizing a 24-hour protection claim. The formula is noted as alcohol-based and gentle on hands.*

* 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.