Cimetidine 5% / Ibuprofen 2% / Salicylic Acid 17%
Product Images NDC 72934-1047

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 5% / Ibuprofen 2% / Salicylic Acid 17% (NDC 72934-1047). 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

Aa (2 End)

Aa (2 End)
Side view of a white cylindrical container label for CIMETIDINE 5% / IBUPROFEN 2% / SALICYLIC ACID 17%, showing directions for use and labeler information. The label instructs application as directed by a physician, external use only, with storage details. Manufacturer is Sincerus Florida, LLC, located in Pompano Beach, FL.*
FDA Label Image

Sf (1047 2 Front)

Sf (1047 2 Front)
Packaging label of CIMETIDINE 5% / IBUPROFEN 2% / SALICYLIC ACID 17% gel, 30 grams, from Sincerus Florida, LLC. The label includes the NDC number 72934-1047-2 and states it is a compounded drug made in the USA.*
FDA Label Image

Sd (1047 2 Middle)

Sd (1047 2 Middle)
Label of CIMETIDINE 5% / IBUPROFEN 2% / SALICYLIC ACID 17% gel, manufactured by Sincerus Florida, LLC. The label lists active ingredients: Cimetidine USP 5%, Ibuprofen USP 2%, and Salicylic Acid USP 17%. Inactive ingredients include Krisgel 100, comprising 3% and 73%. The product is labeled as Rx only with lot number 22101ABCDEFG@1 and manufacturing and expiration dates of 01/01/1970.*

* 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.