Hand Sanitizer
Product Images NDC 73517-767

3 FDA label images from Amyris, 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 Hand Sanitizer (NDC 73517-767). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amyris, 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.

FDA Label Image

Lavender20ml

Lavender20ml
Packaging label for OLIKA Ultra Hydrating Hand Sanitizer in a 20 mL (0.6 fl oz) spray bottle. The lavender-scented sanitizer contains 65% ethyl alcohol and claims to be effective against 99.9% of germs with over 300 sprays per bottle. The label highlights key features such as 24-hour hydration with hyaluronic acid, cruelty-free and vegan formulation, and a carabiner clip for portability. Manufacturer is Amyris, Inc, Emeryville, CA.*
FDA Label Image

Lavender30ml

Lavender30ml
OLIKA Ultra Hydrating Hand Sanitizer spray with 65% ethyl alcohol, 30 mL (1.0 fl oz) bottle with lavender scent. The label highlights 24-hour hydration with hyaluronic acid, effectiveness against 99.9% of germs, and more than 500 sprays per bottle. Packaging includes drug facts, warnings, and usage instructions. Manufactured for Amyris, Inc.*
FDA Label Image

Lavendersage90ml

Lavendersage90ml
Packaging label for OLIKA Ultra Hydrating Hand Sanitizer Refill in a 90 mL (3 fl oz) flexible pouch. The product contains 65% ethyl alcohol and offers 24-hour hydration with hyaluronic acid. It features a lavender sage scent and claims effectiveness against 99.9% of germs with over 1500 sprays per refill. Manufactured for Amyris, Inc.*

* 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.