Sunscreen
Product Images NDC 62932-254

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Sunscreen (NDC 62932-254). 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 (Active)

Active (Active)
This is a Drug Facts label of a product which contains Zinc Oxide as an active ingredient with a concentration of 20% and is intended to be used as a sunscreen.*
FDA Label Image

Artwork (Back Label)

Artwork (Back Label)
This is a drug facts label for organic sunscreen lotion from Two Peas Organics, Santa Barbara, CA, that is free from harmful chemicals such as PABA, parabens, phthalates, BPA, oxybenzone, avobenzone, octinoxate, petrolatum, or 1,4-dioxane. It has been certified to NSF/ANSI 305 by QAI, and if used as directed with other sun protection measures, it is effective in preventing sunburn and reducing the risks of skin cancer and early skin aging caused by the sun. The directions state that it should be applied liberally 15 minutes before sun exposure and reapplied after swimming, sweating, or towel drying, and at least every two hours. Children under 6 months of age should not use this product without consulting a doctor. The sunscreen also comes with warnings to avoid applying on damaged or broken skin, keep out of eyes, and out of reach of children. If swallowed, seek medical attention at once. Also, it is advised to limit time in the sun, especially between 10 am and 2 pm and use long-sleeved shirts, pants, hats, and sunglasses to reduce sun exposure risks. The ingredients of this organic sunscreen include certified organic coconut oil, sunflower seed oil, beeswax, candelilla wax, camera wax, shea butter, castor seed oil, vitamin E, cocoa seed butter, and aloe vera juice. This sunscreen is 125 ml, and its UPC number is 7 05464 04255 8.*
FDA Label Image

Directions And Administration (Directions)

Directions And Administration (Directions)
This is a drug fact label for a sunscreen product that provides directions on how to use, precautions, and SPF value. The sunscreen provides a Broad Spectrum, which protects against skin aging and cancer. The label warns not to use the product on damaged skin and to keep it out of reach of children. The sunscreen should be applied 15 minutes before sun exposure, and it should be reapplied every two hours or after sweating, swimming, or towel drying. In case of any rash, it is advised to consult with a doctor. The label also mentions that the sunscreen contains natural ingredients certified as organic.*
FDA Label Image

Front Label (Front Label)

Front Label (Front Label)
This is a description of a product which is a mineral sunscreen with 20% zinc oxide, broad spectrum SPF 30 protection, and water-resistant for up to 80 minutes. The product comes in a 0.5 oz (14 g) container. It is unclear what "TWU:PEAS" and "ORGANICS" refer to.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This is a list of inactive ingredients in a product. The product contains organic Coconut Oil, Sunflower Seed Oil, Beeswax, Candelilla Wax, Carmauba Wax, Shea Butter, Castor Seed Oil, Vitamin E, Cocoa Seed Butter and Aloe Vera Leaf Juice.*
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Otc Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

Otc Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This text provides warnings and precautions for a drug product. It is advised to only use this product externally and to avoid using it on damaged or broken skin. The user should stop using the product and seek medical attention if they experience a rash. Additionally, the product should be kept away from the eyes and children. If accidentally swallowed, it is recommended to seek medical help or contact a poison control center immediately.*
FDA Label Image

Otc Purpose (Purpose)

Otc Purpose (Purpose)
This is a Drug Facts label. The active ingredient in this drug is Zinc Oxide at 20% concentration, which is used as a sunscreen agent.*
FDA Label Image

Indications And Usage (Use)

Indications And Usage (Use)
This text is a description of a sun protection product that helps prevent sunburn and reduces the risk of skin cancer and early skin aging caused by sun exposure, if used as directed with other sun protection measures. It does not provide any specific details about the product, such as its name or ingredients.*
FDA Label Image

Warning (Warnings)

Warning (Warnings)
This is a description for drug facts and warnings. It is recommended for external use only and not to be used on damaged or broken skin. In case of rash, stop use and consult a doctor. Keep the product away from eyes and children. If swallowed, immediate medical assistance should be sought or a Poison Control Center should be contacted.*

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