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)
This text describes a sunscreen product with 10 OX0R 12% .o SURSCTEER as the active ingredient. It serves to prevent sunburn, skin cancer, and early skin aging caused by the sun. The directions advise shaking well before use, applying liberally 15 minutes before sun exposure, and reapplying every 2 hours or after swimming/sweating. Children under 6 months should consult a doctor before use. The product should be protected from excessive heat and direct sun. The formulation also contains various inactive ingredients like Alantoin, Caprylic/Capric Triglyceride, and Tocopherol among others.*
FDA Label Image

Active Ingredients (Active Ingredients)

Active Ingredients (Active Ingredients)
This text provides information about the active ingredient and purpose of a product, which is Zinc Oxide at 12% concentration for sunscreen. This data is typically found on drug facts labels for products such as sunscreens.*
FDA Label Image

Dosage And Administration (Directions)

Dosage And Administration (Directions)
This text provides directions for using a sunscreen, advising to shake well before use, apply liberally 15 minutes before sun exposure, reapply after swimming or sweating, and every 2 hours. It also mentions sun protection measures including wearing sunscreen with SPF 15 or higher, limiting time in the sun, and wearing protective clothing. Additionally, it cautions about the risks of skin cancer and early skin aging due to sun exposure.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
This is a list of inactive ingredients found in a product. The ingredients have a variety of purposes and include extracts like Centella Asiatica Leaf Extract and Citrus Aurantium Dulcis Peel Extract, as well as added compounds such as Capryl Glycol and Tocopherol. These ingredients may be part of a skincare or cosmetic product formulation.*
FDA Label Image

Indications & Usage (Uses)

Indications & Usage (Uses)
This text describes the uses of a product that helps prevent sunburn and reduces the risk of skin cancer and premature skin aging caused by the sun. When used as directed along with other sun protection measures, it further decreases the risk of skin cancer and premature skin aging due to sun exposure.*
FDA Label Image

Keep Out Of Reach Of Children (Warnings)

Keep Out Of Reach Of Children (Warnings)
This is a list of warnings for a product intended for external use. It mentions not using the product on damaged or broken skin, avoiding contact with eyes and seeking medical help if skin rash occurs. It also advises to keep the product out of reach of children and to contact Poison Control Center in case of swallowing.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.