Salicor Patch
Product Images NDC 80425-0592

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Salicor (NDC 80425-0592). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Dosing (Picture1)

A three-panel instructional illustration showing the application process of a transdermal patch. Panel 1 shows a person cutting open a packet or pouch. Panel 2 shows the patch being removed from the packaging. Panel 3 depicts applying the patch onto a person's shoulder.*

FDA Label Image

Ppi Back (Salicor Package Insert Back 092525)

Drug facts and prescribing information for Salicor (triethanolamine salicylate) 40.2 mg/1 transdermal patch. Includes details on local anesthetic interactions, overdose symptoms, use in specific populations (pregnancy, lactation, pediatric), clinical pharmacology, pharmacokinetics, metabolism, nonclinical toxicology, and storage instructions. Manufactured for Clinic Pharma, Las Vegas, NV.*

FDA Label Image

Ppi Front (Salicor Package Insert Front 092525)

Drug facts and warnings text panel for Salicor transdermal system patch containing triethanolamine salicylate 10%. Includes indications, dosage and administration instructions, contraindications, warnings, precautions, adverse reactions, fetal toxicity, and drug interactions. Emphasizes external use only, allergy alerts, risks like methemoglobinemia, and actions to take in case of adverse effects.*

FDA Label Image

Salicor Patch # 15 (Salicor Patch 80425 0592)

Label for Salicor 10% Patch #15 containing triethanolamine salicylate. The label includes directions for storage between 20°C and 25°C, prescription use indication (Rx Only), barcodes, lot number placeholder, expiration date of 08/31/2030, and is labeled by Advanced Rx of Tennessee, LLC in Nashville, TN. Identifies comparison to NDC 80425-0592-01 and source NDC 83881-0501-15 by Clinic Pharma.*

* 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.