Resfriol D Tablet
Product Images NDC 69729-323

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Resfriol D (NDC 69729-323). 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

Resd12 (Resfriold12)

RESFRIOL D tablet packaging label featuring active ingredients Acetaminophen 500 mg, Chlorpheniramine Maleate 4 mg, and Phenylephrine HCl 10 mg. The label indicates the product is an oral cold and allergy relief medicine containing 12 tablets (6 pouches of 2 tablets) by OPMX LLC. The front panel highlights symptom relief includes headache, nasal congestion, sneezing, and itchy, watery eyes. The box includes bilingual English and Spanish text and a barcode with NDC 69729-323-37.*

FDA Label Image

Resd144 (Resfriold144)

RESFRIOL D tablets packaging label for a human OTC oral drug by OPMX LLC. The box highlights a new formula with Acetaminophen 500 mg, Chlorpheniramine Maleate 4 mg, and Phenylephrine HCl 10 mg as active ingredients. The package contains 144 tablets in 72 pouches of 2 tablets each, intended for cold and allergy relief. The label includes bilingual text in English and Spanish.*

FDA Label Image

Resdpou (Resfrioldpouche)

RESFRIOL D tablets label, containing Acetaminophen 500 mg, Chlorpheniramine Maleate 4 mg, and Phenylephrine HCl 10 mg per tablet. The label indicates it is for cold and allergy relief, with a 2-tablet count shown. Distributed by OPMX LLC, made for RRX, the label is bilingual in English and Spanish and includes warnings, usage instructions, and storage information.*

* 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.