Sensicaine Tm Extra
Product Images NDC 67239-0216

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sensicaine Tm Extra (NDC 67239-0216). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safco Dental Supply Co., 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

Label 2

Label 2
This medicated gel contains 200mg Benzocaine and is designed for oral mucosal use only, for temporary pain relief due to minor dental procedures, but should be used as directed by a dentist. The product may cause Methemoglobinemia which can cause reduced oxygen in blood even if you have used it before. It is not appropriate for children under 2 years or for teething. If you notice a severe sore throat that persists for more than 2 days or symptoms that do not improve in 7 days you should see a doctor. It also contains inactive ingredients like flavoring, PEG 3350, PEG 400, Sucralose, and color additives like D&C Red #33, FD&C Red #40, D&C Green #5, FD&C Yellow #5. For any queries, you can contact 800-621-2178 or visit their website.*
FDA Label Image

Principal Display Panel (29.6 mL Jar Label)

Principal Display Panel (29.6 mL Jar Label)
is a useful description: Safco Dental Supply Co. distributes SensiCai, a professional-use, topical anesthetic gel that contains 20% Benzocaine. Each gram of the gel includes between 180-220mg Benzocaine, with a water-soluble base of PEG 3350, PEG 400 U.S.P, flavor, sucralose, and FDEC Red #40. The strawberry-flavored gel is made in the USA and comes in a 1oz (29.6mL) tube labeled with the reorder number 102-0438 and NDC 67239-0216-1.*

* 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.