Caudalie Daily Mineral Sunscreen Broad Spectrum Spf 50 Lotion
Product Images NDC 76296-060

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Caudalie Daily Mineral Sunscreen Broad Spectrum Spf 50 (NDC 76296-060). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caudalie 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

30 mL Inner Label (30 mL Inner Label)

30 mL Inner Label (30 mL Inner Label)
CAUDALIE Daily Mineral Sunscreen Broad Spectrum SPF 50 lotion in a 30 mL (1 Fl. Oz.) container. The front label shows the brand name, SPF 50, and product description in English and French. The back label lists the active ingredient Zinc Oxide 21.1%, usage instructions to shake well before use, contact information, and manufacturing details for Caudalie USA Inc. Dimensions of the label are 58 mm by 37 mm with a 7 mm margin at the top.*
FDA Label Image

30 mL Outer Label_page_1 (30 mL Outer Label Page 1)

30 mL Outer Label_page_1 (30 mL Outer Label Page 1)
CAUDALIE Daily Mineral Sunscreen Broad Spectrum SPF 50 lotion in a 30 mL (1 Fl. Oz.) size. The label highlights Zinc Oxide 21.1% as the active ingredient for sunscreen use. Manufactured for Caudalie USA, Inc., the packaging emphasizes broad spectrum UVA/UVB protection, a lightweight, silicone-free mineral formula suitable for sensitive skin, and directions for use. The label is predominantly yellow with black text and includes Drug Facts and contact information.*
FDA Label Image

30 mL Outer Label_page_2 (30 mL Outer Label Page 2)

30 mL Outer Label_page_2 (30 mL Outer Label Page 2)
Packaging label for CAUDALIE Daily Mineral Sunscreen Broad Spectrum SPF 50 Zinc Oxide lotion. The label features a grayscale vineyard landscape image with the text "Caudalie Spa Vinothérapie, Bordeaux." The right panel displays Drug Facts and a detailed list of inactive ingredients. The label is outlined in teal and yellow, indicating cut and fold lines for box assembly.*
FDA Label Image

50 mL Inner Label (50 mL Inner Label)

50 mL Inner Label (50 mL Inner Label)
CAUDALIE Daily Mineral Sunscreen Broad Spectrum SPF 50 lotion in a 50 mL (1.7 Fl. Oz.) tube. The front label highlights the SPF 50 with broad spectrum UVA/UVB protection, Vinosun Protect, brightening ingredients including Viniferine and Niacinamide. The back label states it is 100% silicone-free, zinc oxide mineral formula, fragrance-free, with 21.1% active Zinc Oxide. Manufactured for Caudalie USA, Inc.*
FDA Label Image

50 mL Outer Label (50 mL Outer Label)

50 mL Outer Label (50 mL Outer Label)
Packaging label for CAUDALIE Daily Mineral Sunscreen Broad Spectrum SPF 50 lotion containing 50 mL (1.7 fl oz). The sunscreen active ingredient is Zinc Oxide at 21.1%. Labeler is Caudalie USA, Inc., manufactured in the USA. The label includes drug facts with active ingredients, uses, warnings, directions, and a list of inactive ingredients. It also highlights features such as 100% silicone-free, fragrance-free, non-comedogenic, and suitability for sensitive skin.*
FDA Label Image

Copack Label (Copack Label)

Copack Label (Copack Label)
CAUDALIE Daily Mineral Sunscreen Broad Spectrum SPF 50 lotion label packaging in yellow with blue text. The label shows the product name, concentration of Zinc Oxide (21.1%), and states it is a broad spectrum sunscreen for topical use. It includes images of the product bottle and box, with stated volume of 30 mL (1 fl. oz.). The label highlights the sunscreen's dual role as a dark spot brightening serum and sunscreen protection. Manufacturer is Caudalie USA, Inc.*

* 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.