Gelato Topical Anesthetic Spray, Metered
Product Images NDC 68400-323

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Gelato Topical Anesthetic (NDC 68400-323). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mycone Dental Supply Co., Inc Dba Keystone Industries And Deepak Products Inc, 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

Bx.gelato Topical Metered Spray.jpg (Bx.gelato Topical Metered Spray)

This is a drug facts label for a topical anesthetic spray that contains 20% benzocaine with peppermint flavor. It is used for temporary relief of oral pain associated with canker sores and minor irritation. The dosage is a single spray of 50mg. The label lists important warnings and precautions for proper use, such as not using it if you have allergies to similar local anesthetics. The product may cause methemoglobinemia, a serious condition that reduces the amount of oxygen carried in the blood. The product should be used only on oral mucosa to prevent pain. Other ingredients include ethyl alcohol, flavor, polyethylene glycol, sodium saccharin, and hydrocarbon propellant. The manufacturer is Keystone Industries and it is made in the USA.*

FDA Label Image

Lb.metered Spray 99088504

This product is a topical anesthetic spray containing Benzocaine 20%, intended for professional use only, and used for the temporary relief of occasional minor irritation and pain associated with canker sores and minor dental procedures. However, it poses a methemoglobinemia warning and must never be used for teething or by children under the age of 2. In case of overdose, immediate medical attention is recommended. The product should be stored at room temperature and then disposed of according to local regulations. The inactive ingredients include Ethyl Alcohol, Flavor, Polyethylene Glycol, Sodium Saccharin, Hydrocarbon Propellant (sobutane and propane). It shouldn't be used by anyone who has ever had an allergy to any local anesthetics. It's also flammable, so it should be kept away from fire, and smoking should be avoided during use.*

* 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.