Perricone Md Hypoallergenic Cbd Sensitive Skin Therapy Ultra-lightweight Calming Spf 35 Veil Cream
Product Images NDC 84448-615

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Perricone Md Hypoallergenic Cbd Sensitive Skin Therapy Ultra-lightweight Calming Spf 35 Veil (NDC 84448-615). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Thg Beauty Usa 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.

Product Images & Figures Index

FDA Label Image

Package Label Principal Display Panel (Package Label Principal Display Panel)

Package Label Principal Display Panel (Package Label Principal Display Panel)
Label artwork for Perricone MD Hypoallergenic CBD Sensitive Skin Therapy Ultra-Lightweight Calming SPF 35 Veil cream in a 1.7 oz (50 mL) tube. The label highlights the product as a broad spectrum SPF 35 sunscreen containing 15.45% Zinc Oxide. It features detailed Drug Facts, ingredient lists, usage directions, and product branding by THG Beauty USA LLC. The UPC code 651473712633 is visible on the label. The artwork includes measurements for the print dimensions and instructions regarding gloss and matte finishes.*
FDA Label Image

15ml (Screenshot 2025 11 03 161806)

15ml (Screenshot 2025 11 03 161806)
Label for Perricone MD Hypoallergenic CBD Sensitive Skin Therapy Ultra-Lightweight Calming SPF 35 Veil cream, 15 mL (0.5 US fl. oz.) topical product by THG Beauty USA LLC. Contains Zinc Oxide 15.45% as the active ingredient. Includes Drug Facts panel with uses, warnings, directions, and inactive ingredients. UPC barcode and contact information also shown.*

* 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.