Naked Sundays Beautyscreen Peptide Foundation Tint Lotion
Product Images NDC 81104-664

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Naked Sundays Beautyscreen Peptide Foundation Tint (NDC 81104-664). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Naked Sundays, 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)

Pdp (Pdp)
Drug Facts panel for Naked Sundays BeautyScreen Peptide Foundation Tint with Zinc Oxide 12% as the active ingredient. The panel includes sections on active ingredients, uses, warnings, directions, sun protection measures, inactive ingredients, storage instructions, and contact information.*
FDA Label Image

Active Ingredients (Active Ingredients)

Active Ingredients (Active Ingredients)
Drug Facts panel showing active ingredient Zinc Oxide 12% with its purpose listed as sunscreen. The panel is small and formatted in a boxed layout with a gradient background.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
A drug facts or directions panel focused on sun protection use. It includes instructions to shake well and apply liberally 15 minutes before sun exposure, reapplying every 2 hours, and using water-resistant sunscreen if swimming or sweating. It also covers sun protection measures and precautions, such as limiting time in the sun, wearing protective clothing, and consulting a doctor for children under 6 months of age.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
Drug Facts panel listing inactive ingredients for Naked Sundays BeautyScreen Peptide Foundation Tint lotion. Ingredients include Water, C12-15 Alkyl Benzoate, Butylated Salicylate, Isododecane, Lauryl PEG-8 Dimethicone, Propanediol, Titanium Dioxide, Caprylyl Methicone, Dimethicone, Niacinamide, Octyldodecyl Neopentanoate, Polymethylsilsesquioxane, Iron Oxides, Triethoxycaprylylsilane, and others.*
FDA Label Image

Indication & Usage (Uses)

Indication & Usage (Uses)
A portion of a drug facts label displaying the 'Uses' section for a topical zinc oxide product, stating it helps prevent sunburn and may decrease the risk of skin cancer and early skin aging caused by the sun when used as directed with other sun protection measures.*
FDA Label Image

Keep Out Of Reach Of Children (Warning)

Keep Out Of Reach Of Children (Warning)
A small rectangular text panel containing warnings for external use only, advising against use on damaged or broken skin, avoiding prolonged sun exposure, rinsing eyes if contacted, keeping out of children's reach, and stopping use with medical advice if rashes occur or if the product is 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.