5-Symptom Digestive Relief

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: 5-Symptom Digestive Relief
Generic name: BISMUTH SUBSALICYLATE
Manufacturer: TARGET CORPORATION
Product type: HUMAN OTC DRUG
SPL set ID: 28fba615-48ca-8d96-e063-6394a90a2797
SPL ID: 32932e3f-edb6-5d92-e063-6394a90a4c43
Version: 2
Effective date: 2025-04-12
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:26:45

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M008	openfda.application_number
brand name		5-Symptom Digestive Relief	openfda.brand_name
generic name		BISMUTH SUBSALICYLATE	openfda.generic_name
manufacturer name		TARGET CORPORATION	openfda.manufacturer_name
ndc	package	11673-291-08	openfda.package_ndc
ndc	package	11673-291-07	openfda.package_ndc
ndc	package	11673-291-06	openfda.package_ndc
ndc	product	11673-291	openfda.product_ndc
ndc11	package	11673029106	derived:openfda.package_ndc
ndc11	package	11673029107	derived:openfda.package_ndc
ndc11	package	11673029108	derived:openfda.package_ndc
rxcui		308762	openfda.rxcui
spl id		32932e3f-edb6-5d92-e063-6394a90a4c43	id
spl set id		28fba615-48ca-8d96-e063-6394a90a2797	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. Allergy alert: Contains salicylate. Do not take if you are ■ allergic to salicylates (including aspirin) ■ taking other salicylate products

Reported adverse events (FAERS/openFDA)#

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