Diamond Luminous Uv Defense Light Tinted Fluid Sunscreen Broad Spectrum Spf 40 Lotion
Product Images NDC 63730-001

10 FDA label images from Natura Bisse International Sa · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Diamond Luminous Uv Defense Light Tinted Fluid Sunscreen Broad Spectrum Spf 40 (NDC 63730-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Natura Bisse International Sa, 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

63730-001-01 Label (63730 001 01 Label)

63730-001-01 Label (63730 001 01 Label)
Drug Facts panel for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 lotion by Natura Bisse International SA. Lists active ingredients titanium dioxide 7.8% and zinc oxide 25%, both as sunscreens. Includes warnings, directions for use, sun protection measures, inactive ingredients, and contact information for questions. Highlights use for preventing sunburn and reducing skin cancer risk when used as directed.*
FDA Label Image

63730-001-02 Inner Label (63730 001 02 Inner Label)

63730-001-02 Inner Label (63730 001 02 Inner Label)
Label for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 by Natura Bissé. The label lists active ingredients as Titanium Dioxide 7.8% and Zinc Oxide 25%. It specifies a 10 ml (0.3 fl. oz.) lotion with UVA-UVB protection and mineral filters. The product is made in Spain by Natura Bissé International S.A. and is not for individual sale.*
FDA Label Image

63730-001-02 Label (63730 001 02 Label)

63730-001-02 Label (63730 001 02 Label)
This image displays the product information and usage instructions for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 by Natura Bissé International SA. It includes directions for use, precautions, and a description of its all-mineral filters, benefits, and unique features such as brightening, hydration, rejuvenating effects, and a lightweight tinted fluid formula. The text emphasizes broad-spectrum UVA/UVB protection with titanium dioxide and zinc oxide as active mineral filters.*
FDA Label Image

63730-001-02 Outer Label (63730 001 02 Outer Label)

63730-001-02 Outer Label (63730 001 02 Outer Label)
Packaging label for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 lotion by Natura Bisse International SA. The label shows active ingredients titanium dioxide 7.8% and zinc oxide 25%, product volume 0.3 fl. oz. (10 ml), directions for use, warnings, inactive ingredients list, and manufacturer information. The product provides UVA and UVB protection with mineral filters.*
FDA Label Image

63730-001-03 Outer Label (63730 001 03 Outer Label)

63730-001-03 Outer Label (63730 001 03 Outer Label)
Packaging label for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 lotion by Natura Bissé International SA. The label includes drug facts with active ingredients Titanium dioxide 7.8% and Zinc oxide 25%, along with uses, warnings, directions, and a list of inactive ingredients. The package size is 1 FL. OZ. (30 ml) and indicates mineral filters and UVA-UVB protection. Made in Spain by Natura Bissé Int. S.A.*
FDA Label Image

63730-001-03 Inner Label (63730 001 03 Inner Label)

63730-001-03 Inner Label (63730 001 03 Inner Label)
Label of Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 lotion by Natura Bissé International SA. The label lists active ingredients as Titanium Dioxide 7.8% and Zinc Oxide 25%, and notes the 1 fl. oz. (30 ml) package size. Manufactured in Spain, this topical sunscreen provides UVA and UVB protection with mineral filters.*
FDA Label Image

63730-001-03 Label (63730 001 03 Label)

63730-001-03 Label (63730 001 03 Label)
Drug information panel for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 by Natura Bissé International SA. The text includes usage instructions, precautions, product benefits, and formulation details such as use of mineral filters titanium dioxide and zinc oxide. It highlights moisturizing, brightening, hydration, and adaptation to multiple skin tones, along with warnings about sun exposure and irritation.*
FDA Label Image

63730-001-04 Outer Label (63730 001 04 Outer Label)

63730-001-04 Outer Label (63730 001 04 Outer Label)
Packaging label for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 lotion by Natura Bissé International SA. The 1 fl. oz. (30 ml) box highlights active ingredients titanium dioxide 7.8% and zinc oxide 25% as sunscreens. The label includes drug facts, inactive ingredients, directions for use, warnings, and manufacturer information from Barcelona, Spain.*
FDA Label Image

63730-001-04 Inner Label (63730 001 04 Inner Label)

63730-001-04 Inner Label (63730 001 04 Inner Label)
Label for Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 lotion by Natura Bissé International. It lists active ingredients Titanium Dioxide 7.8% and Zinc Oxide 25%, with a package volume of 1 fl oz (30 ml). The product is made in Spain by Natura Bissé Int. S.A. in Barcelona.*
FDA Label Image

63730-001-04 Label (63730 001 04 Label)

63730-001-04 Label (63730 001 04 Label)
This image shows text panels from the Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40 by Natura Bissé International S.A. It includes sections on product description, benefits, mineral protection, hydration, color and texture, precautions, and usage instructions, emphasizing its formulation with all-mineral filters titanium dioxide and zinc oxide, and suitability for daily topical use as a tinted fluid sunscreen.*

* 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.