Childrens Ibuprofen Suspension
Product Images NDC 52412-911

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 Childrens Ibuprofen (NDC 52412-911). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Randob Labs., Ltd., 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

Package Label-principal Display Panel 4 Fl Oz (120 mL) Container Label (Ibuprofen Berry Fig1)

Package Label-principal Display Panel 4 Fl Oz (120 mL) Container Label (Ibuprofen Berry Fig1)
The label for Pediatric Care CHILDREN'S IBUPROFEN Oral Suspension USP contains 100 mg of ibuprofen per 5 mL. It is a pain reliever and fever reducer (NSAID) intended for children ages 2 to 11 years. The label highlights that it is alcohol-free, lasts up to 8 hours, and has a berry flavor. The bottle size is 4 FL OZ (120 mL), and the labeler is Randob Labs., Ltd. The label also includes dosage instructions, warnings, active ingredients, and storage information.*
FDA Label Image

Package Label-principal Display Panel 4 Fl Oz (120 mL) Carton Label (Ibuprofen Berry Fig2)

Package Label-principal Display Panel 4 Fl Oz (120 mL) Carton Label (Ibuprofen Berry Fig2)
Pedia Care CHILDRENS IBUPROFEN Oral Suspension 100 mg/5 mL, berry flavor, in a 4 FL OZ (120 mL) bottle. This over-the-counter oral suspension is indicated for children ages 2 to 11 years and is a pain reliever/fever reducer NSAID. The label highlights alcohol-free formulation and duration of up to 8 hours. Manufactured by Randob Labs., Ltd.*

* 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.