No7 Radiant Glow Foundation Sunscreen Spf 15 Buff
Product Images NDC 68472-096

2 FDA label images from Boots Retail Usa Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for No7 Radiant Glow Foundation Sunscreen Spf 15 Buff (NDC 68472-096). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Boots Retail Usa Inc, 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

Radiant Glow Fdn Carton (Radiant Glow Fdn Carton)

Radiant Glow Fdn Carton (Radiant Glow Fdn Carton)
No7 Radiant Glow Foundation Sunscreen SPF 15 Buff 15 packaging label. The front panel features the product name with a natural luminous finish claim and a 30 mL (1 US Fl. Oz.) volume indication. The label includes Drug Facts with active ingredients Octinoxate 5% and Titanium Dioxide 1.6%, usage instructions, warnings, and an extensive list of inactive ingredients. The labeler is Boots Retail USA Inc. Additional details mention hypo-allergenic properties and directions for application.*
FDA Label Image

Radiant Glow Fnd Bottle Labels (Radiant Glow Fnd Bottle Labels)

Radiant Glow Fnd Bottle Labels (Radiant Glow Fnd Bottle Labels)
Label for No7 Radiant Glow Foundation Sunscreen SPF 15 Buff 15 by Boots Retail USA Inc. The label includes product name, SPF 15, hypo-allergenic claim, active ingredients (Octinoxate 5%, Titanium Dioxide 1.6%), usage instructions, and contact information. The volume is indicated as 30 ml (1 US FL. Oz). The label also mentions non-pore blocking and light-reflecting moisturizing properties.*

* 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.