FDA.reportPublic FDA data

Stomach Relief

Product NDC
17856-1286
11-digit product format
178561286
Labeler code
17856
Product ID
17856-1286_34f36bfa-3ffc-825c-e063-6394a90a45b9
Type
HUMAN OTC DRUG
Nonproprietary name
Bismuth subsalicylate
Dosage form
LIQUID
Route
ORAL
Labeler
ATLANTIC BIOLOGICALS CORP.
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-03-29
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

Additional Listing Data#

Finished product
Yes
Brand name base
Stomach Relief
Brand name suffix
Regular Strength
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BISMUTH SUBSALICYLATE525 mg/30mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii62TEY51RR1
Rxcui308762

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17856-1286-12024-04-19C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-22024-04-19C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-12024-01-30C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-22024-01-30C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-12022-05-19C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-22022-05-19C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-12022-01-28C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts
17856-1286-22022-01-28C16284748780-1d6a99b39-e38a-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-1286-1Stomach ReliefRegular Strength50 in 1 BOX, UNIT-DOSELIQUID505
17856-1286-2Stomach ReliefRegular Strength50 in 1 BOX, UNIT-DOSELIQUID505
17856-1286-3Stomach ReliefRegular Strength15 mL in 1 CUP, UNIT-DOSELIQUID155
17856-1286-4Stomach ReliefRegular Strength30 mL in 1 CUP, UNIT-DOSELIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-1286STOMACH RELIEF REGULAR STRENGTH (BISMUTH SUBSALICYLATE) LIQUID [ATLANTIC BIOLOGICALS CORP.]5Current NDC, Legacy NDC, 4 package rows20250514_5c02d0ba-91e4-4bd2-ac66-6905323653b2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308762bismuth subsalicylate 525 MG in 30 mL Oral SuspensionPSN5c02d0ba-91e4-4bd2-ac66-6905323653b25
308762bismuth subsalicylate 17.5 MG/ML Oral SuspensionSCD5c02d0ba-91e4-4bd2-ac66-6905323653b25
308762bismuth subsalicylate 1.75 % Oral SuspensionSY5c02d0ba-91e4-4bd2-ac66-6905323653b25
308762bismuth subsalicylate 262 MG per 15 ML Oral SuspensionSY5c02d0ba-91e4-4bd2-ac66-6905323653b25
308762bismuth subsalicylate 524 MG per 30 ML Oral SuspensionSY5c02d0ba-91e4-4bd2-ac66-6905323653b25
308762bismuth subsalicylate 525 MG per 30 ML Oral SuspensionSY5c02d0ba-91e4-4bd2-ac66-6905323653b25

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17856-1286-11785612860150 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1286-1) / 15 mL in 1 CUP, UNIT-DOSE (17856-1286-3) 2024-04-180000-00-00NoNoCurrent
17856-1286-21785612860250 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1286-2) / 30 mL in 1 CUP, UNIT-DOSE (17856-1286-4) 2024-04-180000-00-00NoNoCurrent
17856-1286-31785612860315 mL in 1 CUP, UNIT-DOSE15 mlHistorical
17856-1286-41785612860430 mL in 1 CUP, UNIT-DOSE30 mlHistorical