Sealuxe Hand Sanitizer
Product Images NDC 79959-001

3 FDA label images from Apr Beauty Group Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sealuxe Hand Sanitizer (NDC 79959-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apr Beauty Group Inc., 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

1 (1)

1 (1)
SeaLuxe Hand Sanitizer packaging label showing 8 FL OZ (240 mL) volume. The label highlights moisturizing properties, aloe infusion, vitamin E content, and contains bilingual English-French text. It states the product is made in Canada by APR Beauty Group Inc. The back panel lists ethyl alcohol 70% v/v as the active ingredient and includes directions, uses, warnings, and contact information.*
FDA Label Image

2 (2)

2 (2)
Label for SeaLuxe Hand Sanitizer by APR Beauty Group Inc., showing a 10.5 FL OZ (315 mL) bottle. The label highlights moisturizing properties, killing harmful bacteria and germs, infusion with aloe, and vitamin E content. It includes a Drug Facts panel detailing the active ingredient (70% ethyl alcohol) and usage instructions, along with manufacturing information in Canada.*
FDA Label Image

3 (3)

3 (3)
Packaging label for SeaLuxe Hand Sanitizer by APR Beauty Group Inc. The label states it contains 16.9 FL OZ (500 mL) and highlights features such as moisturizing, aloe infusion, and vitamin E. It also mentions killing harmful bacteria and germs and is made in Canada. The label includes drug facts and usage instructions in English and French.*

* 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.