Ibuprofen Pm Capsule, Liquid Filled
FDA Label NDC 41250-285

17 label sections · Submitted to the FDA by Meijer Distribution Inc. · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution Inc. for the product Ibuprofen Pm (NDC 41250-285). 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 ingredients (in each capsule), purposes, uses, warnings, do not use, ask a doctor before use if, ask a doctor or pharmacist before use if you are, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

TAMPER EVIDENT:DO NOT USE IF CARTON IS OPENED OR IF PRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

READ AND KEEP CARTON FOR COMPLETE WARNINGS AND INFORMATION

DIST. MEIJER DISTRIBUTION, INC.

GRAND RAPIDS, MI 49544

www.meijer.com

PID 5138779


†This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare
and Catalent Pharma Solutions, Inc., respective owners of the registered trademarks Advil®
and LIQUI-GELS®.

L0000851 R0424

* Please review the disclaimer below.