Sunscreen
Product Images NDC 62932-217

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Sunscreen (NDC 62932-217). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Private Label Select Ltd Co, 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

Display Carton (Display Carton)

Packaging label for Vertra Reef Safe Lip Balm SPF 15, coconut flavor, distributed by Vertra. The label features Reef Safe branding emphasizing oxybenzone-free, octinoxate-free, and certified organic ingredients including various seed oils and butters. The box dimensions are indicated as 50.8 mm by 75.7 mm, and the label includes a barcode and contact information for Vertra in Torrance, CA.*

FDA Label Image

Dosage And Administration (Dosage)

Text panel showing part of the directions for use and a heading for inactive ingredients of a sunscreen product by Private Label Select Ltd CO. It includes instructions to reapply at least every 2 hours and to ask a doctor for children under 6 months of age.*

FDA Label Image

Inactive Ingredients (Inactive)

Drug Facts panel listing inactive ingredients for SUNSCREEN by Private Label Select Ltd CO. Ingredients include Helianthus Annuus (Sunflower) Seed Oil, Cera Alba (Beeswax), Caprylic/Capric Triglyceride, Cocos Nucifera (Coconut) Oil, Natural Flavors, Polyhydroxystearic Acid, Butyrospermum Parkii (Shea) Butter, Rubus Idaeus (Red Raspberry) Seed Oil, Theobroma Cacao (Cocoa) Seed Butter, Tocopherol, Simmondsia Chinensis (Jojoba) Oil, and Calophyllum Inophyllum (Tamanu) Seed Oil.*

FDA Label Image

Indications And Usage (Indications And Usage)

A drug facts panel section titled 'Uses' describing the product's role in helping to prevent sunburn and reducing 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

Label (Label)

Drug Facts label panel for a sunscreen product by Vertra Premium Suncare. It lists the active ingredient as Zinc Oxide (10.50%) with a purpose of sunscreen, including usage instructions, warnings, directions, inactive ingredients, additional information, and contact details for questions or comments. The label includes SPF 15, broad spectrum, and water resistance for 80 minutes.*

FDA Label Image

Otc Active Ingredient (Otc Active)

A Drug Facts panel listing active ingredients and purpose. It specifies Zinc Oxide (10.50%) as the active ingredient with the purpose of Sunscreen.*

FDA Label Image

Otc Keep Put Of Reach Of Children (Otc Kor)

A warning panel for a sunscreen product by Private Label Select Ltd CO. It includes safety instructions such as for external use only, avoidance on damaged or broken skin, keeping out of eyes and rinsing with water if contact occurs, stopping use and consulting a doctor if rash develops, keeping out of reach of children, and seeking medical help or Poison Control Center if swallowed.*

FDA Label Image

Otc Purpose (Otc Purpose)

A Drug Facts label panel highlighting active ingredients and purpose. It lists Zinc Oxide (10.50%) as the active ingredient and identifies its purpose as sunscreen.*

FDA Label Image

Warnings Section (Warnings)

A text panel presenting warnings for external use only. It advises against use on damaged or broken skin, cautions to keep the product out of eyes and rinse with water if contact occurs, instructs to stop use and consult a doctor if a rash appears, and warns to keep out of reach of children with instructions to get medical help or contact a Poison Control Center 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.