Xl-3 Xtreme Liquid
Product Images NDC 76281-305

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Xl-3 Xtreme (NDC 76281-305). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aptapharma 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

Xl 3 Nightime 6 Oz

XL-3 Xtreme Cold and Cough liquid, a 6 FL OZ (177 mL) multi-symptom cold and flu relief oral syrup by AptaPharma Inc. Contains acetaminophen 650 mg, dextromethorphan HBr 30 mg, and doxylamine succinate 12.5 mg per 30 mL dose cup. The label highlights it is cherry-flavored nighttime formula for relief of sneezing, runny nose, cough, sore throat, fever, aches, and pains. Includes Drug Facts panels with warnings, usage directions, and inactive ingredients.*

FDA Label Image

Xl-3 Night Time Xtreme (Xl 3 Night Time Xtreme)

XL-3 Xtreme Cherry Flavor Night Time liquid, 12 FL OZ (354 mL), multi-symptom cold and flu relief by AptaPharma Inc. Contains acetaminophen 650 mg, dextromethorphan HBr 30 mg, doxylamine succinate 12.5 mg per 30 mL dose. Label highlights relief for sneezing, runny nose, fever, aches, pains, cough, and sore throat.*

FDA Label Image

Xl-3 Xtreme 2 (Xl 3 Xtreme 2)

Drug Facts panel for XL-3 Xtreme Cold and Cough liquid, containing acetaminophen 650 mg/30 mL, dextromethorphan HBr 30 mg/30 mL, and doxylamine succinate 12.5 mg/30 mL. The panel includes warnings about liver damage, allergy risk, use restrictions, overdose instructions, usage directions by age, and inactive ingredients. It also mentions advice for use, storage, and provides a contact number for questions or comments.*

* 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.