Sunscreen
Product Images NDC 62932-211

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Sunscreen (NDC 62932-211). 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

Back (Label Back)

Drug Facts panel for Sunscreen by Private Label Select Ltd CO showing active ingredient Zinc Oxide 20% and listing additional ingredients such as sunflower seed oil and coconut oil. The label includes bilingual English and French text describing product benefits, usage directions, warnings, and safety information, emphasizing prevention of sunburns and appropriate application instructions including timing and frequency.*

FDA Label Image

Front (Label Front)

Label for Thinksport Sunscreen with 30+ SPF, containing 20% zinc oxide as the active ingredient. The label indicates it's a sport formula designed for kids, offering broad-spectrum protection and 80 minutes of water resistance. Net weight is 18.4 grams (0.64 oz). The label is bilingual in English and French and includes the NPN 80083619.*

FDA Label Image

Keep Out Of Reach (Label Keep Out Of Reach)

A drug facts or warning text panel in English and French advising to keep the product out of reach of children and to seek medical help or contact a Poison Control Center if swallowed. It also recommends protecting the product from excessive heat and direct sunlight.*

FDA Label Image

Active (Unit Carton Active Ingredients)

A text panel showing the active ingredient zinc oxide 20% (non-nano) for a sunscreen product, along with bilingual labeling in English and French. The panel also states the product type as sunscreen and notes the size as .64 oz.*

FDA Label Image

Dosage (Unit Carton Dosage)

Directions and sun protection measures for the Sunscreen product by Private Label Select Ltd CO. Instructions include applying sunscreen liberally 15 minutes before sun exposure and reapplying every 2 hours or after swimming, sweating, or towel drying. Sun protection advice highlights limiting sun exposure between 10am and 2pm, wearing protective clothing, and consulting a doctor for children under 6 months. The text is provided in both English and French.*

FDA Label Image

Inactive Ingredients (Unit Carton Inactive)

Ingredient list for a sunscreen product by Private Label Select Ltd CO, including sunflower seed oil, coconut oil, beeswax, candelilla wax, castor oil, carnauba wax, shea butter, cocoa seed butter, vitamin E (tocopherol), aloe leaf juice, papaya fruit extract, and lychee extract.*

FDA Label Image

Indications (Unit Carton Indications And Usage)

The image shows a bilingual drug facts panel for Sunscreen containing Zinc Oxide 20% as the active ingredient. It includes sections on product use, warning, directions for application, and sun protection measures, written in English and French. The directions advise applying liberally 15 minutes before sun exposure and reapplying every 2 hours or after swimming or sweating.*

FDA Label Image

Purpose (Unit Carton Purpose)

A text panel listing the active ingredient as Zinc Oxide 20% (non-nano) and indicating the product is a sunscreen with a specified quantity of 0.64 oz. The panel shows bilingual use instructions in English and French.*

FDA Label Image

Warnings (Unit Carton Warnings)

A warning panel for a sunscreen product from Private Label Select Ltd CO, advising external use only, not to use on damaged or broken skin, to stop use and consult a doctor if rash occurs, and to avoid contact with eyes. Instructions include rinsing with water if contact with eyes happens. The warning is presented in both English and French.*

* 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.