Diclofenac Epolamine
Product Images NDC 50436-3727

4 FDA label images from Unit Dose Services · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diclofenac Epolamine (NDC 50436-3727). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Chemical Structure (Diclofenac 01)

Chemical Structure (Diclofenac 01)
Chemical structure diagram of the active ingredient diclofenac epolamine, showing molecular structures for diclofenac and epolamine components with labeled functional groups and atoms.*
FDA Label Image

Figure 1 And 2 (Diclofenac 02)

Figure 1 And 2 (Diclofenac 02)
Two graphs depicting patient response to diclofenac epolamine patch versus placebo in a 14-day study. Figure 1 shows percent of patients achieving various levels of pain relief on day 3. Figure 2 shows similar data at the end of the study. Both graphs plot percent improvement from baseline against percent of patients improved, with diclofenac patch consistently showing higher improvement than placebo.*
FDA Label Image

Figure 3 And 4 (Diclofenac 03)

Figure 3 And 4 (Diclofenac 03)
Two line graphs comparing percent improvement from baseline to percent of patients improved for diclofenac patch versus placebo. The left graph shows patients achieving various levels of pain relief at day 3 in a 7-day study, while the right graph shows results at the end of the study. Both graphs indicate higher patient improvement percentages with diclofenac patch compared to placebo.*
FDA Label Image

Label Image (Lbl504363727)

Label Image (Lbl504363727)
Label for diclofenac epolamine topical system containing 1.3% topical strength. The label includes NDC 50436-3727-1 and states it is for topical use only. Manufactured or distributed by Unit Dose Services, LLC, located in Dania, Florida. Additional information includes dispensing and warning instructions, a barcode, and various lot and expiration placeholders. Marked as prescription use only (RX only).*

* 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.