Hurricaine Liquid
Product Images NDC 0283-0569

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hurricaine (NDC 0283-0569). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Beutlich Pharmaceuticals, 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

2ct Hsg2 703 0518

Packaging label for HurriCaine Topical Anesthetic Liquid, 20% Benzocaine, OTC oral anesthetic in liquid form. The product is labeled for dental, oral, and periodontal use and comes in 0.005 fl oz Snap-n-Go Swabs, with 2 individually wrapped swabs per package. The label highlights fast relief of oral pain including dentures, sore gums, cold sores, orthodontics, and canker sores. Manufactured by Beutlich Pharmaceuticals, LLC in Bunnell, FL.*

FDA Label Image

72ct Hcs 326 0518

The packaging label for HurriCaine Snap-n-Go Swabs, a 20% benzocaine liquid oral anesthetic in OTC strength. The label indicates an original wild cherry flavor and contains 72 individually wrapped swabs, each with 0.005 fl. oz. (0.15 mL). Manufactured by Beutlich Pharmaceuticals, LLC, the label features usage directions, drug facts, warnings, and application instructions with an image of the swab.*

FDA Label Image

Cherry Liquid Lod 237 0518

HurriCaine Topical Anesthetic Liquid 20% Benzocaine oral anesthetic in Original Wild Cherry flavor from Beutlich Pharmaceuticals, LLC. The 1 fl. oz. carton displays drug facts, warnings, directions, inactive ingredients, and contact information. It is indicated for dental, oral, and periodontal topical use to relieve minor oral pain and irritation.*

* 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.