Sunscreen
Product Images NDC 62932-215

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Sunscreen (NDC 62932-215). 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

Active Ingredients (Active Ingredients)

This text is a product abbreviation and it shows the active ingredient of the product which is Zinc Oxide 20%. Based on this information alone, it is not possible to determine what type of product it is or what it is used for.*

FDA Label Image

Back Label (Back Label)

This is a mineral sunscreen with organic ingredients and an SPF of 30. It contains 20% Zinc Oxide as an active ingredient which helps prevent sunburn, skin cancer, and early skin aging caused by the sun. Its other inactive ingredients include Caprylic/Capric Triglyceride, Sunflower Seed Oil, Candelilla Wax, Castor Seed Oil, Cocoa Seed Butter, and Aloe Vera Leaf Juice among others. It also comes with directions and warnings printed on the packaging. It is distributed by OLITA Inc. in California and is certified organic by NSF/ANSI 305.*

FDA Label Image

Dosage & Administration (Dosage And Administration)

This is a sunscreen product with instructions on how to use it. The sunscreen should be applied generously and evenly 15 minutes before sun exposure. Children under 6 months of age should consult a doctor. Spending time in the sun can increase the risk of skin cancer and premature aging, so users should limit time in the sun, wear protective clothing, and use a sunscreen with an SPF of 15 or higher. Users should also reapply the sunscreen every 80 minutes of swimming or sweating, immediately after towel-drying, and at least every 2 hours.*

FDA Label Image

Front Label (Front Label)

The product is a mineral sunscreen called Coco Bronze Tint with SPF 30 and is water-resistant for up to 80 minutes. It contains organic ingredients.*

FDA Label Image

Inactive Ingredients (Inactive Ingredients)

This is a list of inactive ingredients which includes Caprylic/Capric Triglyceride®, Helianthus Annlus (Sunflower) Seed Qil*, Cera Alba f(Beeswax)”, Euphorbia Cerifera g}oandelllla) Wax, pernicia Cerifera g}amauba) Wax*, utyrospermum Parkii gsglea) utter”, Ricinus mmunis (Castor) Seed Qil*, Tocopherol, Theobroma Cacao (Cocoa) Seed Butter®, Aloe Barbadensis Leaf Juice (Aloe Vera) Powder”, Mica (Ci:77019,), Iron Oxides 492; (Ci77491). The product needs to be protected from excessive heat and direct sun.*

FDA Label Image

Indications & Usage (Indications And Usage)

This text is the description of a product that helps to prevent sunburn. It states that if used correctly with other sun protection measures, it can decrease the risk of skin cancer and early skin aging caused by the sun.*

FDA Label Image

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

FDA Label Image

Purpose (Purpose)

The text seems to be a single word that says "Purpose Sunscreen". Therefore, the description would be that it refers to a type of sunscreen product, but no further information is available.*

FDA Label Image

Warnings Part One (Warnings Part One)

FDA Label Image

Warnings Part Two (Warnings Part Two)

This text seems to be a continuation of a section titled "Drug Facts". It provides instructions to stop using the product and consult a doctor if some kind of issue occurs. There is a warning to keep the product out of reach of children and to seek medical help or poison control center immediately if ingestion occurs. Some of the text is not readable due to errors.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.