FDA.reportPublic FDA data

Maximum strength Stomach Relief

Product NDC
69842-528
11-digit product format
698420528
Labeler code
69842
Product ID
69842-528_6e37d3f7-9589-427c-ae57-03b39833caf9
Type
HUMAN OTC DRUG
Nonproprietary name
Bismuth Subsalicylate
Dosage form
LIQUID
Route
ORAL
Labeler
CVS
Application
part335
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2008-09-08
Substance
BISMUTH SUBSALICYLATE
Active strength
525 mg/30mL
Pharmacologic classes
Bismuth [CS], Bismuth [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Maximum strength Stomach Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BISMUTH SUBSALICYLATE525 mg/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
62TEY51RR1Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
308762Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
75326a55-7cf3-411e-96a3-a6aef6c35ca5Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-528-04Maximum strength Stomach Relief236 mL in 1 BOTTLELIQUID2361
69842-528-05Maximum strength Stomach Relief355 mL in 1 BOTTLELIQUID3551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-528MAXIMUM STRENGTH STOMACH RELIEF (BISMUTH SUBSALICYLATE) LIQUID [CVS]1Current NDC, Legacy NDC, 2 package rows20170808_75326a55-7cf3-411e-96a3-a6aef6c35ca5.zip

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
Maximum strength Stomach ReliefBISMUTH SUBSALICYLATECVS75326a55-7cf3-411e-96a3-a6aef6c35ca52017-08-08WarningsExact identifier
ndc (product): 69842-528

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308762bismuth subsalicylate 525 MG in 30 mL Oral SuspensionPSN75326a55-7cf3-411e-96a3-a6aef6c35ca51
308762bismuth subsalicylate 17.5 MG/ML Oral SuspensionSCD75326a55-7cf3-411e-96a3-a6aef6c35ca51
308762bismuth subsalicylate 1.75 % Oral SuspensionSY75326a55-7cf3-411e-96a3-a6aef6c35ca51
308762bismuth subsalicylate 262 MG per 15 ML Oral SuspensionSY75326a55-7cf3-411e-96a3-a6aef6c35ca51
308762bismuth subsalicylate 524 MG per 30 ML Oral SuspensionSY75326a55-7cf3-411e-96a3-a6aef6c35ca51
308762bismuth subsalicylate 525 MG per 30 ML Oral SuspensionSY75326a55-7cf3-411e-96a3-a6aef6c35ca51

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-528-0469842052804236 mL in 1 BOTTLE (69842-528-04) 236 ml2008-09-080000-00-00NoNoCurrent
69842-528-0569842052805355 mL in 1 BOTTLE (69842-528-05) 355 ml2008-09-080000-00-00NoNoCurrent