Dibucaine Hcl 0.5% / Lidocaine 15% / Phenylephrine Hcl 1% / Prilocaine 5%
Product Images NDC 72934-5071

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dibucaine Hcl 0.5% / Lidocaine 15% / Phenylephrine Hcl 1% / Prilocaine 5% (NDC 72934-5071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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

Ds (5071 4 End)

The image shows a white cylindrical container with a label that includes directions for use and contact information. The product name DIBUCAINE HCL 0.5% / LIDOCAINE 15% / PHENYLEPHRINE HCL 1% / PRILOCAINE 5% is not explicitly visible on the label. The label provides instructions to apply topically as directed by a physician, lists storage conditions, and includes the labeler Sincerus Florida, LLC with a phone number and address in Pompan Beach, FL. A QR code is also present on the label.*

FDA Label Image

S (5071 4 Front)

DIBUCAINE HCL 0.5% / LIDOCAINE 15% / PHENYLEPHRINE HCL 1% / PRILOCAINE 5% ointment in a white cylindrical container with a label displaying the active ingredients and their strengths. The label also shows the NDC 72934-5071-4, the manufacturer Sincerus Florida, LLC, and the product weight of 120 grams. The label notes it is a compounded drug made in the USA.*

FDA Label Image

F (5071 4 Middle)

Packaging label of DIBUCAINE HCL 0.5% / LIDOCAINE 15% / PHENYLEPHRINE HCL 1% / PRILOCAINE 5% ointment. The label lists the active ingredients with their respective concentrations and also mentions oleabase plasticized as an inactive ingredient. The label includes the Rx only status, lot number, manufacturing date, and labeler Sincerus Florida, LLC.*

* 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.