Cimetidine 10% / Lidocaine 5% / Salicylic Acid 40%
Product Images NDC 72934-2046

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 Cimetidine 10% / Lidocaine 5% / Salicylic Acid 40% (NDC 72934-2046). 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

C (2046 2 End)

C (2046 2 End)
A white cylindrical container showing a label panel with directions for use stating application as directed by a physician, washing hands after use, external use only, and storage at controlled room temperature (20-25°C). Manufacturer contact information for Sincerus Florida, LLC in Pompano Beach, FL, with phone numbers and FDA reporting details, is also visible on the label.*
FDA Label Image

F (2046 2 Front)

F (2046 2 Front)
The image shows a white cylindrical cream container labeled with the proprietary name CIMETIDINE 10%, LIDOCAINE 5%, SALICYLIC ACID 40% cream in a 30 gram size. The label indicates it is a compounded drug made in the USA and bears the logo and name of the labeler, Sincerus Florida, LLC. The NDC number 72934-2046-2 is also visible on the label.*
FDA Label Image

D (2046 2 Middle)

D (2046 2 Middle)
Label from CIMETIDINE 10%, LIDOCAINE 5%, SALICYLIC ACID 40% topical product by Sincerus Florida, LLC. The label lists active ingredients with their USP percentages: Cimetidine 10%, Lidocaine 5%, and Salicylic Acid 40%. Inactive ingredients include Butylated Hydroxytoluene, Salt Stable LS Cream, and Vitamin E Acetate.*

* 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.