Blume Sunburst Sunscreen Lotion
Product Images NDC 83656-2106

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 Blume Sunburst Sunscreen (NDC 83656-2106). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blume, 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

Pdp (Pdp)

Pdp (Pdp)
Drug Facts panel for Blume Sunburst Sunscreen with Zinc Oxide 12%. The panel includes active ingredient purpose, uses, warnings, directions for application, other information about product storage, and a detailed list of inactive ingredients.*
FDA Label Image

Active Ingredients (Active Ingredients)

Active Ingredients (Active Ingredients)
Drug Facts panel showing the active ingredient Zinc Oxide 12%, listed with the purpose Sunscreen. The panel is a simple table format under the heading 'Drug Facts.'*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
Directions panel for Blume Sunburst Sunscreen Zinc Oxide 132 mg/mL lotion. Instructions include shaking well before use, applying 15 minutes before sun exposure, reapplying after swimming, sweating, or towel drying, and at least every 2 hours. It advises consulting a doctor for children under 6 months and notes sun protection measures to reduce skin cancer and aging risks.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This image shows the inactive ingredients list for Blume Sunburst Sunscreen lotion with Zinc Oxide 132 mg/mL. It includes various extracts, oils, esters, and other compounds such as allantoin, bisabolol, caprylic/capric triglyceride, citrus peel extracts and oils, coconut fruit extract, sunflower extract, jojoba esters, niacinamide, rosemary leaf extract, silica, sodium chloride, tocopherol, and water, among others.*
FDA Label Image

Indications & Usage (Uses)

Indications & Usage (Uses)
This Drug Facts panel section titled 'Uses' states that the product helps prevent sunburn and decreases the risk of skin cancer and early skin aging caused by the sun. It notes that using the product as directed with other sun protection measures further decreases these risks.*
FDA Label Image

Keep Out Of Reach Of Children (Warnings)

Keep Out Of Reach Of Children (Warnings)
Warning label panel for Blume Sunburst Sunscreen zinc oxide lotion includes warnings for external use only, not to use on damaged or broken skin, to keep out of eyes and rinse with water if contact occurs, to stop use and ask a doctor if a skin rash occurs, to keep out of reach of children, and to get medical help or contact a 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.