Dr Loretta Universal Glow Daily Defense Spf 40 Cream
Product Images NDC 71501-1910

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dr Loretta Universal Glow Daily Defense Spf 40 (NDC 71501-1910). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Loretta, Llc, 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

Label0 (Label0)

This is a description of a mineral sunscreen fluid with broad-spectrum SPF 40 and PA+++. This formula contains anti-aging skincare benefits, acts as a lightweight moisturizer, and provides protection from the sun. It is recommended to apply the product liberally and evenly 15 minutes before sun exposure and to reapply at least every 2 hours. The active ingredient is Zinc Oxide at 17%. The formula also includes a variety of other ingredients such as Shea Butter, Ectoin, Lavender Oil, and extracts like Birch Bark and Gotu Kola. The product is made in the USA and comes in a 0.5 fl oz / 15mL sample size.*

FDA Label Image

Label2 (Label2)

This product is a Mineral Sunscreen Fluid with Broad Spectrum SPF40. It contains 17% Zinc Oxide as the active ingredient for sun protection. The sunscreen is recommended to be applied liberally and evenly 15 minutes before sun exposure and reapplied at least every 2 hours. It is water-resistant and provides protection against skin aging and skin cancer risks. The product is distributed by Dr. Loretta, LLC and is intended for professional use only. It includes various inactive ingredients and is packaged in a 3.41 fl oz / 100 mL container.*

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