Equaline Maximum Strength Stomach 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: Equaline Maximum Strength Stomach Relief
Generic name: BISMUTH SUBSALICYLATE
Manufacturer: UNITED NATURAL FOODS, INC. DBA UNFI
Product type: HUMAN OTC DRUG
SPL set ID: 716a7b86-4f6e-493d-ba29-d81f6ecafbf2
SPL ID: 10fda877-8724-4525-ac12-5406a18ad601
Version: 5
Effective date: 2024-12-20
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:52:53

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M008	openfda.application_number
brand name		Equaline Maximum Strength Stomach Relief	openfda.brand_name
generic name		BISMUTH SUBSALICYLATE	openfda.generic_name
manufacturer name		UNITED NATURAL FOODS, INC. DBA UNFI	openfda.manufacturer_name
ndc	package	41163-937-04	openfda.package_ndc
ndc	package	41163-937-05	openfda.package_ndc
ndc	product	41163-937	openfda.product_ndc
ndc11	package	41163093705	derived:openfda.package_ndc
ndc11	package	41163093704	derived:openfda.package_ndc
rxcui		308763	openfda.rxcui
spl id		10fda877-8724-4525-ac12-5406a18ad601	id
spl set id		716a7b86-4f6e-493d-ba29-d81f6ecafbf2	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.