Coldtac Severe Cold Capsule, Liquid Filled
Product Images NDC 69729-808

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Coldtac Severe Cold (NDC 69729-808). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Opmx 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

Pdp (Coldtac Severe Cold Max Relief 001)

Pdp (Coldtac Severe Cold Max Relief 001)
The packaging label for Coldtac Severe Cold Max Relief capsules, liquid filled, contains active ingredients Acetaminophen 325 mg and Dextromethorphan HBr 10 mg. The label displays the brand name Coldtac Severe Cold prominently with Max Relief in a yellow box. It includes bilingual cold and flu relief indications, highlighting headache, sore throat, fever reducer, and cough suppressant. The package size is 10 soft gels. The labeler is OPMX LLC, with distribution noted for RRX.*
FDA Label Image

Esp (Coldtac Severe Cold Max Relief 002)

Esp (Coldtac Severe Cold Max Relief 002)
Drug facts panel in Spanish for Coldtac Severe Cold Max Relief capsules, showing active ingredients Acetaminophen 325 mg and Dextromethorphan HBr 10 mg, purpose, uses, warnings including liver and allergy alerts, directions, additional information, and inactive ingredients. The panel advises consulting a doctor for certain conditions and contains standard OTC medication warnings and usage instructions.*

* 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.