Sun Protection Spf 50 Spray
Product Images NDC 83694-011

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Sun Protection Spf 50 (NDC 83694-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Skinresource.md, L.l.c., 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 Ingredients (Active Ingredient)

Partial Drug Facts panel listing active ingredients and their concentrations for Sun Protection SPF 50 topical spray: Avobenzone 2.9%, Homosalate 4.0%, Octisalate 4.9%, and Octocrylene 9.5%.*

FDA Label Image

Package Label (Classic Spray Spf 50)

Label for Sun Protection Spray SPF 50 by Skinresource.md, L.L.C., a human OTC topical spray sunscreen containing Avobenzone 2.9%, Homosalate 4.0%, Octisalate 4.9%, and Octocrylene 9.5%. The 6 fl. oz. (177 mL) water-resistant spray bottle includes dermatologist-approved and no animal testing logos. The label provides drug facts with active ingredients, purpose, warnings, directions, and contact information.*

FDA Label Image

Dosage And Administration (Dosage And Administration)

Text panel containing directions and sun protection measures for Sun Protection SPF 50 topical spray. Directions advise applying liberally 15 minutes before sun exposure and reapplying every 2 hours or after swimming/sweating. Sun protection measures mention risk reduction by using broad spectrum SPF 15 or higher sunscreen and additional protective actions.*

FDA Label Image

Inactive Ingredients (Inactive Ingredients)

A text panel listing inactive ingredients of Sun Protection SPF 50 spray. It includes Acrylates/Octylacrylamide Copolymer, Alcohol Denat, Aloe Barbadensis Leaf Extract, Butyloctyl Salicylate, Carthamus Tinctorius (Safflower) Seed Oil, Ethyl Ferulate, Helianthus Annuus (Sunflower) Seed Oil, Polyester-8, and Tocopherol, with an asterisk marking certified organic ingredients.*

FDA Label Image

Indications And Usage (Indications And Usage)

This image shows a drug facts panel for a topical sun protection spray. It includes sections on uses, warnings (flammability, external use only, avoid damaged skin and eyes), directions for use, precautions for children, and sun protection measures to reduce risks of skin cancer and early skin aging.*

FDA Label Image

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

A warning text panel advising to keep the product out of reach of children and to seek medical help or contact a Poison Control Center immediately if the product is swallowed.*

FDA Label Image

Purpose (Purpose)

Drug Facts panel of Sun Protection SPF 50 topical spray, listing active ingredients including Avobenzone 2.9%, Homosalate 4.0%, Octisalate 4.9%, and Octocrylene 9.5%. The panel includes the Purpose section identifying the product as a sunscreen.*

FDA Label Image

Warnings (Warnings)

A warning panel for a topical spray product, including instructions such as 'For external use only,' 'Flammable - Do not spray near heat, sparks, sources of ignition, or flames,' and to protect the product from excessive heat and direct sun. Additional warnings advise not to use on damaged or broken skin, to keep out of eyes and rinse with water if contact occurs, and to stop use and consult a doctor if skin irritation or redness persists for more than 72 hours.*

* 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.