Acqua Aroma Hand Sanitizer Gel
Product Images NDC 70848-413

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acqua Aroma Hand Sanitizer Gel (NDC 70848-413). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Smell It Industria E Comercio Ltda, 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

Use (Drugfacts 1 Floz)

Drug Facts panel for Acqua Aroma Hand Sanitizer Gel 1.0 FL OZ (30 mL) listing Ethyl Alcohol 70% as the active antiseptic ingredient. Includes warnings about flammability, external use, and keeping out of reach of children. Directions advise rubbing into hands until dry. The panel also lists inactive ingredients, storage temperature, and manufacturer details from Smell It Industria e Comercio Ltda.*

FDA Label Image

Acqua Aroma (Primary Panel 12 9 Floz)

Drug Facts panel for Acqua Aroma Hand Sanitizer Gel 12.9 FL OZ (380 mL) by Smell It Industria e Comercio Ltda. Includes active ingredient ethyl alcohol 70%, usage directions, warnings, inactive ingredients list, and manufacturing information. The panel also shows branding text "The scent of your home," NDC number 70848-413-80, and product claims like killing 99.9% of common bacteria.*

FDA Label Image

Acqua Aroma (Primarypanel 1 Floz)

Packaging label for Acqua Aroma Hand Sanitizer Gel, featuring 1.0 FL OZ (30 mL) volume. The label highlights the inclusion of Vitamin E microspheres and states that the product kills 99.9% of common bacteria. The label also displays the NDC number 70848-410-30, with the labeler identified as Smell It Industria e Comercio Ltda.*

* 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.