Ibuprofen Tablet
FDA Label NDC 69848-011

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Granules Usa, Inc. for the product Ibuprofen (NDC 69848-011). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient (for tablet), active ingredient (for caplet), purpose, uses, allergy alert:, stomach bleeding warning:, heart attack and stroke warning:, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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