Pepto Bismol Chews

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Pepto Bismol Chews
Generic name: BISMUTH SUBSALICYLATE
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: cfe9214d-25e9-7729-e053-2a95a90a0dfb
SPL ID: 579c459a-830c-dc48-e063-6294a90a45bc
Version: 15
Effective date: 2026-07-27
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:08

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M008	openfda.application_number
brand name		Pepto Bismol Chews	openfda.brand_name
generic name		BISMUTH SUBSALICYLATE	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	69423-963-72	openfda.package_ndc
ndc	package	69423-963-24	openfda.package_ndc
ndc	package	69423-963-48	openfda.package_ndc
ndc	product	69423-963	openfda.product_ndc
ndc11	package	69423096372	derived:openfda.package_ndc
ndc11	package	69423096348	derived:openfda.package_ndc
ndc11	package	69423096324	derived:openfda.package_ndc
rxcui		211151	openfda.rxcui
rxcui		308761	openfda.rxcui
spl id		579c459a-830c-dc48-e063-6294a90a45bc	id
spl set id		cfe9214d-25e9-7729-e053-2a95a90a0dfb	set_id
unii		62TEY51RR1	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings 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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.