Pepto Bismol Capsule, Liquid Filled
FDA Label NDC 37000-537

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Pepto Bismol (NDC 37000-537). 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 other, active ingredient (in each liquicap), purpose, uses, reye's syndrome, allergy alert:, otc - do not use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

MADE IN CANADA

DIST. BY PROCTER & GAMBLE,

CINCINNATI OH 45202

Reye's Syndrome

Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

* Please review the disclaimer below.