FDA.reportPublic FDA data

WALGREENS

Product NDC
0363-1834
11-digit product format
003631834
Labeler code
0363
Product ID
0363-1834_2de7ff66-af75-4d9d-b493-29b37dadc5d8
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium citrate dihydrate
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
WALGREENS CO.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-12-29
Substance
TRISODIUM CITRATE DIHYDRATE
Active strength
230 mg/1
Pharmacologic classes
Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
WALGREENS
Brand name suffix
UPSET STOMACH and NAUSEA RELIEF
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TRISODIUM CITRATE DIHYDRATE230 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
B22547B95KInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2002800Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2de7ff66-af75-4d9d-b493-29b37dadc5d8Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-1834-42WALGREENSUPSET STOMACH and NAUSEA RELIEF1 in 1 BOXTABLET, CHEWABLE11
0363-1834-42WALGREENSUPSET STOMACH and NAUSEA RELIEF42 in 1 BOTTLETABLET, CHEWABLE421

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WALGREENS UPSET STOMACH and NAUSEA RELIEFSODIUM CITRATE DIHYDRATEWALGREENS CO.2de7ff66-af75-4d9d-b493-29b37dadc5d82026-01-15WarningsExact identifier
ndc (product): 0363-1834

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2002800sodium citrate 230 MG Chewable TabletPSN2de7ff66-af75-4d9d-b493-29b37dadc5d81
2002800sodium citrate 230 MG Chewable TabletSCD2de7ff66-af75-4d9d-b493-29b37dadc5d81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0363-1834-42003631834421 BOTTLE in 1 BOX (0363-1834-42) / 42 TABLET, CHEWABLE in 1 BOTTLE1 bottle2025-12-29NoNoCurrent