Acetaminophen Tablet
FDA Label NDC 70518-4783

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Remedyrepack Inc. for the product Acetaminophen (NDC 70518-4783). 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.

Package Label.Principal Display Panel

DRUG: Acetaminophen

GENERIC: Acetaminophen

DOSAGE: TABLET

ADMINSTRATION: ORAL

NDC: 70518-4783-0

COLOR: white

SHAPE: ROUND

SCORE: Two even pieces

SIZE: 12 mm

IMPRINT: 54;27

PACKAGING: 120 in 1 BOTTLE, PLASTIC

ACTIVE INGREDIENT(S):

  • ACETAMINOPHEN 500mg in 1
  • INACTIVE INGREDIENT(S):

    • STARCH, CORN
    • STEARIC ACID
    • POVIDONE K30
    • SODIUM STARCH GLYCOLATE TYPE A POTATO
    • Remedy_label (Remedy Label)

      Remedy_label (Remedy Label)

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