Cabinet Cough Relief
Product Images NDC 68210-6010

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cabinet Cough Relief (NDC 68210-6010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Spirit Pharmaceuticals 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

Cabinet Cought Travel Carton.jpg (Cabinet Cought Travel Carton)

Package label for Cabinet Cough Relief softgels containing Dextromethorphan HBr 15 mg per softgel. The label shows the product name, active ingredient, and quantity of 25 softgels. It includes directions, warnings, inactive ingredients, and storage instructions. The labeler is Spirit Pharmaceuticals LLC, and the product compares to the active ingredient in Robitussin Long Acting Cough Gels. The package includes a barcode and tamper-evident warning.*

FDA Label Image

Cabinet Bottle Label.jpg (Cabinet Bottle Label)

Cabinet Cough Relief contains 15 mg Dextromethorphan HBr in a softgel dosage form. The label indicates a package size of 50 softgels and includes a Drug Facts panel specifying the active ingredient's purpose as a cough suppressant. The product is distributed by Spirit Pharmaceuticals LLC and made in India. The design features orange diagonal stripes on a white background.*

FDA Label Image

Cabinet Dextro Travel Label.jpg (Cabinet Dextro Travel Label)

Cabinet Cough Relief packaging label for softgels containing 15 mg Dextromethorphan HBr. The label indicates a package size of 25 softgels and is labeled by Spirit Pharmaceuticals LLC. The design features orange diagonal stripes with usage, warnings, directions, and other regulatory information printed on the label.*

* 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.