WALGREENS UPSET STOMACH and NAUSEA 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: WALGREENS UPSET STOMACH and NAUSEA RELIEF
Generic name: SODIUM CITRATE DIHYDRATE
Manufacturer: WALGREENS CO.
Product type: HUMAN OTC DRUG
SPL set ID: 2de7ff66-af75-4d9d-b493-29b37dadc5d8
SPL ID: 2de7ff66-af75-4d9d-b493-29b37dadc5d8
Version: 1
Effective date: 2026-01-15
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:21

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		WALGREENS UPSET STOMACH and NAUSEA RELIEF	openfda.brand_name
generic name		SODIUM CITRATE DIHYDRATE	openfda.generic_name
manufacturer name		WALGREENS CO.	openfda.manufacturer_name
ndc	package	0363-1834-42	openfda.package_ndc
ndc	product	0363-1834	openfda.product_ndc
ndc11	package	00363183442	derived:openfda.package_ndc
rxcui		2002800	openfda.rxcui
spl id		2de7ff66-af75-4d9d-b493-29b37dadc5d8	id
spl set id		2de7ff66-af75-4d9d-b493-29b37dadc5d8	set_id
unii		B22547B95K	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 Do not use if you ▪ have Hereditary Fructose Intolerance (HFI). This product contains fructose. Ask a doctor before use if you ▪ have diabetes because this product contains sugar ▪ are on a sodium-restricted diet Ask a doctor or pharmacist before use if you ▪ are taking any other medications. This product may interact with certain prescription drugs. When using this product, ▪ do not take more than 24 tablets in a 24-hour period. Stop use and ask a doctor if ▪ nausea lasts more than two weeks or recurs frequently. If pregnant or breast-feeding, ▪ ask a health professional before use. Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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