Pentrexcilina Suspension
Product Images NDC 69729-824

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pentrexcilina (NDC 69729-824). 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

Bottle (Pentrexcilina Bottle)

Bottle (Pentrexcilina Bottle)
Label for Pentrexcilina Fever Infant Acetaminophen oral suspension, 160 mg/5 mL, cherry flavor, by OPMX LLC. The 2 fl oz (60 mL) bottle label highlights it as a pain reliever and fever reducer safe for infants aged 2-3 years, dye free and paraben free. Drug facts and dosing instructions are included in detail.*
FDA Label Image

Df Esp (Pentrexcilina Esp)

Df Esp (Pentrexcilina Esp)
The image shows the drug facts and medication information panel for Pentrexcilina, an acetaminophen 160 mg/5 mL oral suspension. The text is in Spanish and includes sections on active ingredient, temporary uses, warnings about liver damage and allergies, dosage guidelines by weight and age, storage instructions, inactive ingredients, and a contact number for questions or comments.*
FDA Label Image

Pdp1 (Pentrexcilina Pdp)

Pdp1 (Pentrexcilina Pdp)
Pentrexcilina Fever Infant Acetaminophen 160 mg/5 mL oral suspension in a 2 fl oz (60 mL) bottle. The packaging features bilingual text in English and Spanish, indicating it is a pain reliever and fever reducer for infants aged 2 to 3 years. It is cherry flavored and labeled as dye and paraben free, manufactured by OPMX LLC and made in India.*

* 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.