Stellalife Hand Sanitizer Liquid
Product Images NDC 69685-201

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Stellalife Hand Sanitizer (NDC 69685-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stellalife, 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.

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FDA Label Image

Ndc: 69685-201-28 (Otc Hand Sanitizer Label Front Panel Display Stellalife)

Ndc: 69685-201-28 (Otc Hand Sanitizer Label Front Panel Display Stellalife)
This is a drug facts label for a hand sanitizer which contains 70% ethyl alcohol as its active ingredient. The product is intended to reduce bacteria that may lead to disease when soap and water are unavailable. The label includes warnings such as keeping the sanitizer away from heat, flames, eyes, ears, mouth and children younger than 2 months. The sanitizer should not be used on open wounds. If irritation or rash occurs, consumers are advised to stop using it and consult with a doctor. Users should supervise children under 6 years of age while using the sanitizer. The sanitizer also contains aloe vera extract, Frankincense oil, Lemon grass oil, lavender oil, Tea tree oil and Vitamin E oil as inactive ingredients. It should be stored between 15-30C (59-86F) and protected from freezing and excessive heat above 40C (104F).*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.