Lavaderm Aftersun Spray
Product Images NDC 70631-067

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Lavaderm Aftersun (NDC 70631-067). 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

Active Ingredient (Active Ingredient Box)

Label for LavaDerm AfterSun Spray by Young Living Essential Oils, LC, containing Menthol 0.5% topical analgesic in a 2 oz (57 g) spray form. The label highlights pain and itch relief features, specifies usage instructions, warnings, inactive ingredients, and distributor information including contact and recycling instructions.*

FDA Label Image

Active Ingredient (Principal Display Panel)

Drug Facts panel for LavaDerm AfterSun spray containing 0.5% menthol as the active ingredient. The label outlines uses for temporary relief of pain and itching due to minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations. It includes warnings, directions for use by adults and children, storage instructions, and contact information for questions. Additional manufacturer info and product marketing text are also present.*

* 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.