Green Goo Hand Sanitizer
Product Images NDC 70994-336

2 FDA label images from Sierra Sage Herbs, Llc · 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 Green Goo Hand Sanitizer (NDC 70994-336). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sierra Sage Herbs, Llc, 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

Natural_lavender_1.jpg (Natural Lavender 1)

Natural_lavender_1.jpg (Natural Lavender 1)
The Blue packaging label for Green Goo Hand Sanitizer lavender scent shows the proprietary name and specifies it contains 1.0 fl. oz. (29.5 ml). It highlights key features such as being made from sugarcane, 100% recyclable, ISO certified, FDA approved, and BPA free. The manufacturer is Sierra Sage Herbs LLC located in Lyons, Colorado. The label includes a Drug Facts panel with 70% ethyl alcohol as the active ingredient and additional usage, warnings, directions, and inactive ingredients information.*
FDA Label Image

Natural_lavender_3.jpg (Natural Lavender 3)

Natural_lavender_3.jpg (Natural Lavender 3)
The packaging label for Green Goo Hand Sanitizer, Lavender scent, featuring 3.0 fl. oz. (88.5 mL) in a tube made from 100% sugarcane. The label highlights the product's natural ingredients including 70% alcohol as the active ingredient and describes its floral aroma. It notes that the sanitizer is 100% recyclable, ISO certified, FDA approved, and BPA free. The label includes a Drug Facts panel, usage directions, and product/company information for Sierra Sage Herbs, LLC, based in Lyons, CO, USA.*

* 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.