Tabcin Active Capsule, Liquid Filled
Product Images NDC 69729-809

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tabcin Active (NDC 69729-809). 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

Pdp1 (Tabcin Active W10 Red Softgel (en Es) Glue Rev. 12.2025 001)

Label for tabcin ACTIVE, containing Acetaminophen and Dextromethorphan HBr in a liquid-filled capsule dosage form. The package contains 10 softgel capsules. It is labeled as non-drowsy and for cough and flu multi-symptom relief. The labeler is OPMX LLC. The NDC is 69729-809-10.*

FDA Label Image

Tabla Drug Facts Eng (Tabla Drug Facts Eng Tabcin Active)

Drug Facts panel for tabcin ACTIVE softgels containing acetaminophen 325 mg as pain reliever/fever reducer and dextromethorphan HBr 10 mg as cough suppressant. The panel includes uses, warnings, directions, overdose information, and inactive ingredients. It advises on dose limits, liver warnings, allergy alerts, and advises consulting a doctor for certain conditions.*

FDA Label Image

Tabla Drug Facts Eng (Tabla Drug Facts Esp Tabcin Active)

Pharmacological information panel in Spanish for tabcin ACTIVE Capsules, liquid filled, containing acetaminophen 325 mg and dextromethorphan HBr 10 mg per capsule. The panel lists active ingredients, purposes, uses, warnings including liver warnings and allergy alerts, and dosing instructions for different age groups. Additional information includes inactive ingredients and a contact phone number for questions.*

* 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.