Lavaderm After Sun
Product Images NDC 70631-034

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Lavaderm After Sun (NDC 70631-034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Young Living Essential Oils, Lc, 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

Label (720673lavadermaftersunv2usaol)

Drug Facts panel for Lavaderm After Sun For Pain and Itching spray by Young Living Essential Oils. It lists menthol 0.5% as the active ingredient for topical analgesic use. The label details uses, warnings, directions, storage, and company contact information, and describes the product as a 100% plant-based formula for temporary relief of pain and itching due to minor burns, sunburn, cuts, scrapes, insect bites, and minor skin irritation.*

FDA Label Image

Box (820673bxlavadermaftersunboxv2usaol)

Drug Facts panel for Lavaderm After Sun Spray by Young Living Essential Oils, LC, listing menthol 0.5% as active ingredient for topical analgesic use. Provides detailed usage instructions, warnings, and inactive ingredient list. Additional text describes product benefits for pain and itching relief from minor burns, sunburn, cuts, scrapes, insect bites, with a moisturizing, non-sticky formula. Includes manufacturer contact details and recycling notice.*

* 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.