Ibuprofen
Product Images NDC 63868-281

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 63868-281). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association Inc., 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 Front 40ct (Cdma15 01 Back)

A drug facts panel for Ibuprofen outlining warnings about taking other NSAIDs, aspirin, or blood thinners concurrently. It advises on the risk of heart attack and stroke, and instructs not to exceed the recommended dosage or duration. Directions caution against use by children under 12 years or adults requiring more than 1 capsule every 6 hours for more than 10 days, with instructions to consult a doctor if symptoms persist or worsen. The labeler is Chain Drug Marketing Association Inc.*

FDA Label Image

Bottle Front 40ct (Cdma15 01 Front)

Ibuprofen Liquid Filled Softgels label showing 200 mg strength. The packaging identifies the product as ibuprofen capsules, a pain reliever and fever reducer NSAID. The carton contains 40 softgels and is manufactured by Chain Drug Marketing Association Inc., with NDC 63868-281-40. The label includes usage instructions, warnings, and storage information.*

FDA Label Image

Carton Back 40ct (Cdma16 01 Back)

Drug Facts panels for Ibuprofen capsules from Chain Drug Marketing Association Inc. detailing active ingredient and purpose, uses, warnings including allergy information, stomach bleeding warnings, heart attack/stroke warnings, and advice for special populations such as pregnant or breastfeeding women. Instructions for use and warnings to stop use and consult a doctor under certain conditions are also included.*

FDA Label Image

Carton Front 40ct (Cdma16 01 Front)

The packaging label for Ibuprofen Liquid Filled Softgels by Chain Drug Marketing Association Inc. features 200 mg ibuprofen capsules, a pain reliever and fever reducer (NSAID). The box contains 40 softgels. The label includes directions, inactive ingredients, storage instructions, and a barcode. The product compares the active ingredient to that in Motrin IB Liquid Gels.*

FDA Label Image

Bottle Front 80ct (Cdma17 01 Back)

A directions panel for ibuprofen capsules stating dosage instructions for adults and children 12 years and over, emphasizing not to exceed recommended amounts and advising consultation with a doctor for children under 12 years or as needed. Includes a toll-free contact number for questions or comments.*

FDA Label Image

Bottle Front 80ct (Cdma17 01 Front)

Ibuprofen Liquid Filled Softgels, 200 mg ibuprofen capsules, shown in an 80 count package. The label indicates the product as a pain reliever and fever reducer NSAID. The labeler is Chain Drug Marketing Association Inc., with warnings and usage instructions printed on the carton.*

FDA Label Image

Carton Back 80ct (Cdma18 01 Back)

Drug Facts panels for Ibuprofen capsules. The text details active ingredient information, uses, warnings including allergy alerts and specific conditions to avoid use, when to ask a doctor, heart attack and stroke warnings, symptoms that require stopping use and medical consultation, as well as instructions regarding pregnancy, children, and overdose. The panels provide safety and usage information for consumers.*

FDA Label Image

Carton Front 80ct (Cdma18 01 Front)

Ibuprofen Liquid Filled Softgels, 200 mg capsules, pain reliever/fever reducer (NSAID) by Chain Drug Marketing Association Inc. The carton contains 80 softgels. The label highlights the active ingredient strength and dosage form, shows a capsule image, and includes comparison to Motrin IB Liquid Gels. The package features branding and regulatory information, including the NDC 63868-281-80.*

* 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.