Suave Hand Sanitizer Professional
Product Images NDC 50069-109

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Suave Hand Sanitizer Professional (NDC 50069-109). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unilever Asia Private Limited, 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

01b Lbl Suave Hand Sani Gel 75pct 1000ml

Drug Facts panel from Suave Hand Sanitizer Professional 33.8 FL OZ (1L) highlights the active ingredient as Ethyl alcohol 75% v/v with antiseptic purpose. It includes usage instructions, warnings about flammability and external use, directions for use, and inactive ingredients. The panel also provides manufacturer and distributor information, safety symbols, and customer contact details.*

FDA Label Image

01b Lbl Suave Hand Sani Gel 75pct 236ml

Suave Hand Sanitizer Professional in an 8 FL OZ (236 mL) plastic bottle. The label shows the product name prominently, with a statement that it kills 99.9% of germs. The active ingredient is alcohol 75%, indicated for antiseptic use. The labeler is Unilever Asia Private Limited. Additional text includes usage warnings, directions, and manufacturing information.*

FDA Label Image

01b Lbl Suave Hand Sani Gel 75pct 500ml

Label of Suave Hand Sanitizer Professional, showing 16.9 FL OZ (500 mL) bottle size. Active ingredient is ethyl alcohol 75% v/v listed as an antiseptic. The label includes usage, warnings, directions, and inactive ingredients. Manufactured by Guangzhou Xufeli Cosmetic Co., Ltd for Unilever Asia Private Limited, with distribution details and contact information.*

* 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.