Omnilux Mineral Facial Sunscreen Lotion
Product Images NDC 83866-1762

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Omnilux Mineral Facial Sunscreen (NDC 83866-1762). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Lotus Global Group, Inc, Dba Globalmed Technologies, 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

Pdp (Pdp)

Drug Facts panel for Omnilux Mineral Facial Sunscreen containing 12% Zinc Oxide. It details active ingredient, uses, warnings, directions for application, other information, inactive ingredients, and contact information. The panel includes instructions on sun protection measures and cautions for use on damaged skin and near eyes.*

FDA Label Image

Active Ingredients (Active Ingredients)

Drug Facts panel listing Zinc Oxide 12% as the active ingredient with the purpose of sunscreen. The panel is minimal and focuses solely on this ingredient and its function.*

FDA Label Image

Dosage And Administration (Directions)

Directions panel for Omnilux Mineral Facial Sunscreen lotion with Zinc Oxide, including instructions to apply 15 minutes before sun exposure, reapply every 2 hours, use water-resistant sunscreen when swimming, and precautions for children under 6 months. Also includes sun protection measures such as using sunscreen with SPF 15 or higher and limiting sun exposure from 10 a.m. to 2 p.m., wearing protective clothing and sunglasses.*

FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Text panel listing inactive ingredients of Omnilux Mineral Facial Sunscreen Zinc Oxide lotion includes water, various triglycerides, esters, glyceryl stearate, squalane, multiple plant extracts, gums, alcohols, tocopherol, sodium hydroxide, iron oxides, and other common formulation agents.*

FDA Label Image

Indications & Usage (Uses)

This image shows a small text box titled 'Uses,' detailing that the product helps prevent sunburn and, when used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.*

FDA Label Image

Keep Out Of Reach Of Children (Warning)

A drug facts warning panel for Omnilux Mineral Facial Sunscreen with Zinc Oxide. It states the product is for external use only, advises against use on damaged or broken skin, instructs to keep out of eyes and rinse with water if contact occurs, advises to stop use and consult a doctor if a rash develops, and emphasizes keeping the product out of reach of children with instructions to seek medical help if swallowed.*

* 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.