Sea And Ski Advanced Hand Sanitizer 8oz
Product Images NDC 73440-2133

2 FDA label images from Cross Brands Contract Filling · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sea And Ski Advanced Hand Sanitizer 8oz (NDC 73440-2133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cross Brands Contract Filling, 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

Active Ingredient (2133 S S Adv Hand Sanitizer Gel 8 Fl Oz Back)

Active Ingredient (2133 S S Adv Hand Sanitizer Gel 8 Fl Oz Back)
Drug Facts panel for Sea and Ski Advanced Hand Sanitizer with 62% alcohol as the active antiseptic ingredient. The panel includes sections on uses, warnings, directions, other information, and inactive ingredients. It provides safety information on flammability, external use, and child supervision, along with storage instructions and manufacturer details (Cross-Brands Contract Filling, Rockledge, FL). A barcode is also visible.*
FDA Label Image

Front (2133 S S Adv Hand Sanitizer Gel 8 Fl Oz Front)

Front (2133 S S Adv Hand Sanitizer Gel 8 Fl Oz Front)
Label of Sea and Ski Advanced Hand Sanitizer 8 oz topical solution. The label highlights moisturizing aloe and contains 62% alcohol antiseptic. The design features a green and blue color scheme with the product name prominently displayed along with an aloe graphic and water splash imagery. The product volume is 8 fl oz (237 mL).*

* 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.