Sanaflu Xtra Capsule, Gelatin Coated
Product Images NDC 48201-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sanaflu Xtra (NDC 48201-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grandall Distributing, 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

Box (Box)

Sanaflu Xtra Adult Flu and Cough capsules packaging label. The label highlights active ingredients acetaminophen, chlorpheniramine maleate, dextromethorphan HBr, and phenylephrine. It indicates the product is a pain reliever, fever reducer, antihistamine, cough suppressant, and nasal decongestant. The package contains 12 gelatin-coated softgel capsules and is distributed by Grandall Distributing, LLC, made in Mexico.*

FDA Label Image

Drug Facts Panel 1 (Drug Facts1)

Drug Facts panel for Sanaflu Xtra capsules listing active ingredients per capsule: Acetaminophen 250 mg, Chlorpheniramine maleate 2 mg, Dextromethorphan HBr 10 mg, and Phenylephrine HCl 5 mg. It outlines uses such as temporary relief of minor aches, headache, runny nose, sneezing, nasal congestion, itchy/watery eyes, coughing, and fever reduction. Warnings include a liver warning related to acetaminophen intake limits and cautions against use with other acetaminophen products or certain prescription drugs.*

FDA Label Image

Drug Facts Panel 2 (Drug Facts2)

Drug Facts panel continuing warnings, directions, other information, and inactive ingredients for Sanaflu Xtra capsule. It includes precautions related to medical conditions, interactions, use instructions for adults and children, storage advice, and a list of inactive ingredients such as colors, gelatin, glycerin, and various polymers.*

* 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.