The Peninsula Hand Sanitizer
Product Images NDC 80176-004

2 FDA label images from Cerci Kozmetik Ve Otel Ekipmanlari Pazarlama Ic Ve Dis Ticaret Limited Sirketi · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for The Peninsula Hand Sanitizer (NDC 80176-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cerci Kozmetik Ve Otel Ekipmanlari Pazarlama Ic Ve Dis Ticaret Limited 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.

Product Images & Figures Index

FDA Label Image

Image Description (Image 2)

Image Description (Image 2)
THE PENINSULA HAND SANITIZER in a 0.50 fl.oz. (15 ml) white squeeze tube with black cap. The front shows the product name, natural aloe and matricaria flower extracts, and net volume. The back displays Drug Facts including the active ingredient Alcohol 70% (v/v), uses, warnings, inactive ingredients, and distributor information from LABOTTEGA USA in New York.*
FDA Label Image

Image Description (Image 1)

Image Description (Image 1)
THE PENINSULA HAND SANITIZER packaging label showing a 0.50 fl. oz. (15 ml) container. The front displays the brand name, product type, and mention of natural aloe and matricaria flower extracts. The back panel includes drug facts such as active ingredient (Alcohol 70% ±5%), purpose (antiseptic), usage instructions, warnings, inactive ingredients, and manufacturer details indicating it is made in Turkey and distributed by Labottega USA in New York.*

* 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.