Banana Boat Lotion
Product Images NDC 63354-312

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Banana Boat (NDC 63354-312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Edgewell Personal Care Brands Llc, 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

Back Label (Back Label Screenshot 2025 12 03 113016)

Drug Facts panel for BANANA BOAT lotion listing active ingredients Avobenzone 2.7%, Homosalate 7.5%, Octisalate 4.5%, Octocrylene 5.0% as sunscreens. Covers uses, warnings, directions for application, and other information like inactive ingredients. Includes safety steps such as applying liberally, waiting 15 minutes, reapplying every 2 hours, and wearing protective clothing. Distributed by Edgewell Personal Care Brands LLC.*

FDA Label Image

Front Label (Front Label Screenshot 2025 12 03 112854)

BANANA BOAT Sheer Sensitive sunscreen lotion with SPF 50, labeled as UVA/UVB broad spectrum. The label highlights dermatologist and pediatrician approval, water resistance for 80 minutes, and fragrance and alcohol-free formulation. The product is in a 0.4 fl. oz. (11.8 mL) container and is by Edgewell Personal Care Brands LLC.*

FDA Label Image

Label (Label Screenshot 2025 12 02 162236)

BANANA BOAT Sheer Sensitive Sunscreen Lotion SPF 50 with active ingredients Avobenzone 2.7%, Homosalate 7.5%, Octisalate 4.5%, and Octocrylene 5.0%. It is dermatologist and pediatrician approved, water resistant for 80 minutes, fragrance and alcohol free, packaged in a 6 fl oz (177 mL) plastic tube. Distributed by Edgewell Personal Care Brands LLC.*

* 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.