Sunscreen
Product Images NDC 62932-218

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 62932-218). 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 Label)

Back Label (Back Label)
This is a sunscreen lotion manufactured by Suntegrity Skincare® in Las Vegas, NV, USA. It is certified to NSF/ANSI 305 by QAI and contains Zinc Oxide (20%) as an active ingredient. The lotion helps prevent sunburn and decreases the risk of skin cancer and early skin aging caused by the sun. The lotion is meant for external use only and should not be applied on damaged or broken skin or swallowed. It should be applied liberally 15 minutes before sun exposure and re-applied after 80 minutes of swimming or sweating or immediately after towel drying, at least every 2 hours. The lotion contains certified organic ingredients and should be protected from excessive heat and direct sun.*
FDA Label Image

Dosage And Administration (Doasge And Administration)

Dosage And Administration (Doasge And Administration)
This is a drug fact sheet for a sunscreen product. It provides instructions on how to use the product to prevent sunburn, skin cancer, and early aging caused by the sun. It warns against using the product on damaged or broken skin, and getting the product in one's eyes. The directions recommend applying the sunscreen 15 minutes before sun exposure and reapplying after swimming or sweating. The product is also only for external use, and parents should consult a doctor before using it on children under six months old. It also lists the inactive ingredients and provides additional information to protect the product from excessive heat and direct sun.*
FDA Label Image

Front Label (Front Label)

Front Label (Front Label)
This is a description for a water-resistant Mineral Sun Stick with Broad Spectrum SPF 30. The product comes in a 1.62oz (46g) package and is suitable for use during sports activities lasting up to 80 minutes.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This product contains a number of inactive ingredients including caprylic/capric triglyceride and various plant oils and waxes (such as sunflower seed oil, beeswax, and shea butter) as well as castor seed oil, cocoa seed butter, and aloe vera juice. It also contains mica and iron oxides for color, and is made with certified organic ingredients.*
FDA Label Image

Indications And Usage (Indications And Usage)

Indications And Usage (Indications And Usage)
This text appears to be the product label or description of a sun protection product. It states that the product helps prevent sunburn and, if used according to the instructions with other sun protection measures, can reduce the risk of skin cancer and early skin aging caused by sun exposure.*
FDA Label Image

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

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
This is a warning label for a topical product that is meant for external use only. The user is advised not to use it on damaged or broken skin, and to stop using it and consult a doctor if a rash occurs. It should be kept out of eyes and the reach of children, and in case of accidental ingestion, medical attention should be sought immediately.*
FDA Label Image

Warnings Section (Warnings)

Warnings Section (Warnings)
This text contains warnings for using a skincare product. It states that the product is only for external use and should not be applied on damaged or broken skin. If a rash occurs or the product enters the eyes, the use of the product should be stopped, and a doctor should be consulted. It is also advised to keep the product away from the reach of children and to seek medical help or contact a Poison Control Center immediately in case of swallowing.*
FDA Label Image

Otc-active Ingredient Section (Active Ingredient Section)

Otc-active Ingredient Section (Active Ingredient Section)
The text is a label information providing the Drug Facts for a product with Zinc Oxide (20%) as the active ingredient used as sunscreen.*
FDA Label Image

Otc-purpose Section (Purpose Section)

Otc-purpose Section (Purpose Section)
This is a drug facts label. The product contains Zinc Oxide as an active ingredient which has a concentration of 20% and is used for sun protection.*

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