The Green Beaver Company Spf 40 Adult Sunscreen
Product Images NDC 76098-003

8 FDA label images from The Green Beaver Company · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for The Green Beaver Company Spf 40 Adult Sunscreen (NDC 76098-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Green Beaver Company, 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

Sunscreen Spf 40 (Spf 40 Us Adult Final Label Pdp)

Sunscreen Spf 40 (Spf 40 Us   Adult   Final Label Pdp)
The Green Beaver Company SPF 40 Adult Sunscreen label displaying natural mineral sunscreen, fragrance-free, broad spectrum SPF 40 protection. The label highlights hypoallergenic, dermatologist tested, water-resistant (40 minutes), and not chalky properties. It includes the brand logo with a beaver and leaf graphic, and states the net weight as 3.3 oz (94 g).*
FDA Label Image

Active Ingredient (Spf 40 Us Adult Final Label Active)

Active Ingredient (Spf 40 Us   Adult   Final Label Active)
A partial drug facts panel listing active ingredients for The Green Beaver Company SPF 40 Adult Sunscreen, showing zinc oxide at 8% and titanium dioxide at 8% concentrations.*
FDA Label Image

Directions (Spf 40 Us Adult Final Label Dosage And Admin)

Directions (Spf 40 Us   Adult   Final Label Dosage And Admin)
The image shows a directions panel for The Green Beaver Company SPF 40 Adult Sunscreen. It provides instructions to apply liberally 15 minutes before sun exposure, advises consulting a doctor for children under 6 months, and includes sun protection measures such as limiting sun exposure time and reapplying after swimming or sweating.*
FDA Label Image

Inactive Ingredients (Spf 40 Us Adult Final Label Inactive)

Inactive Ingredients (Spf 40 Us   Adult   Final Label Inactive)
Text panel listing inactive ingredients of The Green Beaver Company SPF 40 Adult Sunscreen, including Helianthus Annuus (Sunflower) Seed Oil, Dicaprylyl Carbonate, Beeswax, Caprylyl Capric Triglyceride, among others, with mention that ingredients are from organic farming.*
FDA Label Image

Keep Out Of Reach (Spf 40 Us Adult Final Label Keep Out Of Reach)

Keep Out Of Reach (Spf 40 Us   Adult   Final Label Keep Out Of Reach)
A partial view of a product label text panel showing the beginning of the 'Directions' section, printed in green italicized font on a white background. The panel includes usage instructions typical for sunscreen products, focusing on application directions and safety information.*
FDA Label Image

Purpose (Spf 40 Us Adult Final Label Purpose)

Purpose (Spf 40 Us   Adult   Final Label Purpose)
A partial Drug Facts panel showing the section titled Purpose with the word Sunscreen listed twice below it. The text is in blue on a light background.*
FDA Label Image

Uses (Spf 40 Us Adult Final Label Uses)

Uses (Spf 40 Us   Adult   Final Label Uses)
Text panel excerpt from The Green Beaver Company SPF 40 Adult Sunscreen labeling, describing the 'Uses' section which explains that the product helps prevent sunburn and may decrease the risk of skin cancer and skin aging caused by the sun if used as directed with other sun protection measures.*
FDA Label Image

Warnings (Spf 40 Us Adult Final Label Warnings)

Warnings (Spf 40 Us   Adult   Final Label Warnings)
A drug facts text panel showing warnings for The Green Beaver Company SPF 40 Adult Sunscreen. It includes instructions to use externally only, avoid use on damaged or broken skin, keep out of eyes, and rinse with water if contact occurs. It advises to stop use and seek a doctor if rash appears, keep out of reach of children, and contact Poison Control Center if swallowed.*

* 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.