Hurricaine Spray
Product Images NDC 0283-0610

2 FDA label images from Beutlich Pharmaceuticals Llc · 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 Hurricaine (NDC 0283-0610). 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

Ho25b 596 0518 25ct Carton

Ho25b 596 0518 25ct Carton
Drug Facts panel for HurriCaine Topical Anesthetic, 20% benzocaine oral anesthetic, detailing uses, warnings including methemoglobinemia risk, allergy alerts, and dosage directions by age. Includes instructions on storage, inactive ingredients, and contact information. The adjacent Directions panel illustrates how to open, unlock, grasp, position, and spray HurriCaine ONE, with steps 1 through 5 showing pouch opening, unlocking the device, spray positioning, and application technique for dental use.*
FDA Label Image

Ho2b 595 0518 2ct Carton

Ho2b 595 0518 2ct Carton
HurriCaine One Unit Dose Non-Aerosol Spray with 20% Benzocaine oral anesthetic in original wild cherry flavor. Manufactured by Beutlich Pharmaceuticals LLC. The package contains two 0.017 fl. oz. (0.5 mL) unit dose sprays designed for dental and periodontal use. Includes a product diagram showing parts of the spray device and drug facts panel detailing active ingredients, warnings, directions, inactive ingredients, and contact information.*

* 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.