Neogen Dermalogy Day-light Protection Airy Sunscreen Broad Spectrum Spf 50 Cream
Product Images NDC 87471-101

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Neogen Dermalogy Day-light Protection Airy Sunscreen Broad Spectrum Spf 50 (NDC 87471-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Outin Futures Co.,ltd., 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

Neogen_daylight_protection_airy_sunscreen_spf50_ic (Neogen Daylight Protection Airy Sunscreen Spf50 Ic)

Label and tube packaging for NEOGEN DERMALOGY DAY-LIGHT PROTECTION AIRY SUNSCREEN Broad Spectrum SPF 50 cream. The label highlights the product as an advanced sun protection solution with active ingredients Avobenzone 3%, Homosalate 8%, and Octocrylene 8%. The product is distributed by Outin Futures Co., Ltd., and the label includes usage directions, warnings, and drug facts. The packaging shows a gradient orange to blue design with white text and includes a 50 ml (1.69 FL. OZ.) volume indication.*

FDA Label Image

Neogen_daylight_protection_airy_sunscreen_spf50_oc (Neogen Daylight Protection Airy Sunscreen Spf50 Oc)

Packaging label for NEOGEN DERMALOGY DAY-LIGHT PROTECTION AIRY SUNSCREEN Broad Spectrum SPF 50 cream. The label features an orange to blue gradient background with white text detailing active ingredients Avobenzone 3%, Homosalate 8%, Octocrylene 8% as sunscreens. Directions, warnings, and other information appear on the side panel. The product is distributed by Outin Futures Co., Ltd., Seoul, Korea, and made in the USA. Container size is 50 ml (1.69 FL. OZ.).*

* 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.