Texaclear Pain Reliever Liquid
Product Images NDC 58809-389

View Photos of 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 Texaclear Pain Reliever (NDC 58809-389). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gm Pharmaceuticals, Inc, 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

Onsert1

Onsert1
Drug Facts panel for TEXACLEAR PAIN RELIEVER oral liquid, containing active ingredients caffeine 65 mg and choline salicylate 870 mg per 30 mL. The panel details uses, warnings including Reyes syndrome, allergy alerts, stomach bleeding, and recommendations for children, and advises consulting a doctor before use under certain conditions.*
FDA Label Image

Onsert2

Onsert2
Drug Facts panel for TEXACLEAR PAIN RELIEVER liquid containing caffeine and choline salicylate. It includes warnings about stomach bleeding symptoms, pregnancy and breastfeeding precautions, overdose instructions, dosage directions for adults and children, and storage conditions. Lists inactive ingredients like citric acid, glycerin, and sodium saccharin. Provides a customer service phone number for questions or comments.*
FDA Label Image

Principaldisplaylabel

Principaldisplaylabel
Label for TEXACLEAR PAIN RELIEVER liquid containing choline salicylate and caffeine, marked as a fast-acting pain reliever. The label highlights a free & clear formula without dye, sugar, gluten, alcohol, or acetaminophen. The container size is 8 fluid ounces (237 mL) and the product is distributed by GM Pharmaceuticals, Inc., Arlington, TX. The label includes dosage instructions for ages 12+ and dosing intervals.*

* 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.