Childrens Ibuprofen Oral Suspension
Product Images NDC 0121-0833

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 Childrens Ibuprofen Oral Suspension (NDC 0121-0833). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Carton Label (4 oz)

Carton Label (4 oz)
Childrens Ibuprofen Oral Suspension, USP (NSAID) 100 mg per 5 mL in a 4 fl oz (120 mL) bottle, labeled for ages 2 to 11 years. The packaging highlights it is alcohol-free and dye-free, provides pain relief and fever reduction lasting up to 8 hours, and is manufactured by PAI Holdings, LLC dba PAI Pharma. The label includes dosing instructions, warnings, drug facts, and a barcode.*
FDA Label Image

Lidding Label (5 mL)

Lidding Label (5 mL)
Label for Children's Ibuprofen Oral Suspension, USP, 100 mg per 5 mL strength. The label indicates it is an NSAID, shake well before use, and is alcohol and dye free. It is labeled for institutional use only and distributed by PAI Pharma, Greenville, SC. The label also shows a barcode and an NDC number 0121-0833-05.*
FDA Label Image

Lidding Label (10 mL)

Lidding Label (10 mL)
Label for Children’s Ibuprofen Oral Suspension, USP, showing 200 mg per 10 mL strength. The round label directs to shake well before use, states it is alcohol and dye free, and is designated for institutional use only. It includes the NDC number 0121-1666-10 and notes the labeler as PAI Pharma, Greenville, SC.*

* 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.