Acetaminophen Tablet
FDA Label NDC 55154-7897

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health 107, Llc for the product Acetaminophen (NDC 55154-7897). 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 drug facts, otc - purpose, uses, warnings, otc - do not use, otc - ask doctor, otc - ask doctor/pharmacist, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Principal Display Panel

Acetaminophen Extra Strength Tablets

500 mg

10 Tablets

Bag Label (9efcce86 Dd57 4ea2 Ad31 D2038eb61bf1 00)

Bag Label (9efcce86 Dd57 4ea2 Ad31 D2038eb61bf1 00)

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