Lidocaine 30%
Product Images NDC 72934-5141

3 FDA label images from Sincerus Florida, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidocaine 30% (NDC 72934-5141). 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.

Product Images & Figures Index

FDA Label Image

Ds (5141 4 End)

Ds (5141 4 End)
The image shows a white cylindrical container of LIDOCAINE 30% by Sincerus Florida, LLC. The label includes directions for use, advising application as directed by a physician and external use only, with storage instructions at controlled room temperature. Contact information for reporting adverse reactions is provided along with a QR code.*
FDA Label Image

F (5141 4 Front)

F (5141 4 Front)
LIDOCAINE USP 30% ointment in a white cylindrical container with a screw cap. The label shows the active ingredient concentration and the net weight of 120 grams. It is labeled by Sincerus Florida, LLC, with the product NDC 72934-5141-4. The label states the product is a compounded drug made in the USA.*
FDA Label Image

Ds (5141 4 Middle)

Ds (5141 4 Middle)
LIDOCAINE 30% ointment in a white cylindrical container with a label indicating the active ingredient is Lidocaine USP at 30% concentration and inactive ingredients at 70%. Manufactured and labeled by Sincerus Florida, LLC, the label also includes manufacturing and expiration dates along with batch 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.