Pro-tect Sunscreen For Professionals
Product Images NDC 61619-866

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Pro-tect Sunscreen For Professionals (NDC 61619-866). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-cute Derm, Incorporated, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

86608 8oz V 0005.1 06172020 Master Test

86608 8oz V 0005.1 06172020 Master Test
This text is a part of Drug Facts label of a sunscreen product. The sunscreen provides Broad-Spectrum UVA/UVB protection and claims to help prevent sunburns, skin aging, and skin cancer. The sunscreen should be applied liberally 15 minutes before sun exposure and reapplied every two hours and after activities like swimming or sweating. Children under 6 months old must ask a doctor. The product contains inactive ingredients such as Aloe Vera, Benzyl Alcohol, Stearic Acid, etc. The product is greaseless, very water-resistant, fragrance-free, and non-comedogenic. A company named Pro-Spectrum ProcessTM produces the product. The NDC number of the product is 61619-886-08, and the product comes in an 8.0 FL OZ (236.6 mL) container. The product warns that it is for external use only and should not be used on damaged or broken skin. If a rash occurs, a doctor's consultation is required. The product should not get in the eyes and should be removed by rinsing with water. The product should be protected from excessive heat and direct sun. For questions or comments, contact 1-800-922-2883.*

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