Coldtac Ultra Tablet
Product Images NDC 69729-133

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Coldtac Ultra (NDC 69729-133). 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

Cold144 (Coldtac Ultra144vovan)

Packaging label for COLDTAC ULTRA tablets by OPMX LLC, an oral human OTC drug. The label highlights active ingredients acetaminophen 500 mg, chlorpheniramine maleate 4 mg, and phenylephrine HCl 10 mg. The product is marketed as cold and flu relief medicine, presenting bilingual English and Spanish text. The package size indicated is 144 tablets, divided into 72 packs of 2 tablets each, with clear branding and dose information.*

FDA Label Image

Box (Coldtac Ultra 12 Tablets (6 2 Pouches)37)

COLDTAC ULTRA tablets packaging label showing the product name prominently. The active ingredients are Acetaminophen 500 mg, Chlorpheniramine Maleate 4 mg, and Phenylephrine HCl 10 mg. The label indicates the product provides relief for headache, nasal congestion, itchy watery eyes, runny nose, and sneezing. The package contains 12 tablets and is labeled for oral use. It is made for OPMX LLC.*

FDA Label Image

37 Esp (Coldtac Ultra W6 Tablets (3 2 Pouches) En Es (rte) 37 Esp)

Drug Facts panel in Spanish for COLDTAC ULTRA oral tablets containing acetaminophen 500 mg, chlorpheniramine maleate 4 mg, and phenylephrine HCl 10 mg. The label provides active ingredients and their purposes, uses, warnings including liver and allergy alerts, dosing instructions by age, storage information, inactive ingredients, and contact information for questions or comments.*

FDA Label Image

Box2-3 (Coldtac Ultra W6 Tablets (3 2 Pouches))

Packaging label for COLDTAC ULTRA tablets, an oral human OTC drug by OPMX LLC. The label features the brand name prominently and lists active ingredients per tablet: Acetaminophen 500 mg, Chlorpheniramine Maleate 4 mg, and Phenylephrine HCl 10 mg. It indicates the product offers effective and quick relief from cold and flu symptoms such as headache, fever, body aches, sneezing, runny nose, watery eyes, nasal congestion, and sore throat. The package contains 6 tablets divided into 3 packs of 2 tablets each.*

FDA Label Image

Esp (Coldtac Ultra W6 Tablets (3 2 Pouches) Esp)

Drug information panel in Spanish for COLDTAC ULTRA tablets containing acetaminophen 500 mg, chlorpheniramine maleate 4 mg, and phenylephrine HCl 10 mg. The text covers active ingredients, uses, warnings, allergy alert, throat pain warning, drug interactions, usage instructions, overdose warning, additional storage information, inactive ingredients, and contact information for questions or comments.*

FDA Label Image

Cold2 (Coldtac Ultra2vovan)

COLDTAC ULTRA caplets packaging label showing active ingredients per tablet: Acetaminophen 500 mg, Chlorpheniramine Maleate 4 mg, and Phenylephrine HCl 10 mg. The label indicates 2 tablets per package and lists the labeler as OPMX LLC. The design includes warnings, uses, and storage information with bilingual English and Spanish text.*

FDA Label Image

Box100 (Coldtac Ultra 100 Box)

COLDTAC ULTRA 500 mg / 4 mg / 10 mg tablet carton for oral use by OPMX LLC. The label shows the active ingredients acetaminophen (500 mg), chlorpheniramine maleate (4 mg), and phenylephrine HCl (10 mg). The package contains 100 tablets packaged as 50 packs of 2 tablets each. Label text is bilingual in English and Spanish, describing it as cold & flu relief medicine to alleviate symptoms of cold and flu (Gripe y Resfriado).*

* 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.