FDA.reportPublic FDA data

NDC 51596-005-01 - Heartburn Relief to Go

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51596-005
Requested NDC
51596-005-01
Package NDCs from labels
51596-005-10, 51596-005-01, 51596-005-05, 51596-005-12, 51596-005-24
Manufacturer
Breakthrough Products Inc.
Effective date
2014-10-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Heartburn Relief to Go ™Breakthrough Products Inc.2014-10-06HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDCRelated label
51596-005-05Heartburn Relief to Go ™
51596-005-10Heartburn Relief to Go ™
51596-005-12Heartburn Relief to Go ™
51596-005-24Heartburn Relief to Go ™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51596-005-01Heartburn Relief to Go1 in 1 POUCHPOWDER13
51596-005-05Heartburn Relief to Go5 in 1 BOXPOWDER53
51596-005-10Heartburn Relief to Go1 in 1 PACKETPOWDER13
51596-005-10Heartburn Relief to Go10 in 1 BOXPOWDER103
51596-005-12Heartburn Relief to Go12 in 1 BOXPOWDER123
51596-005-24Heartburn Relief to Go24 in 1 BOXPOWDER243

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51596-005HEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.]3Legacy NDC, 6 package rows20141017_88cadd90-c6f4-4229-aed4-bf3e4ce6dbf5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Calcium carbonateACTIVE INGREDIENTH0G9379FGKHEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.]3
carbonate ionACTIVE MOIETY7UJQ5OPE7DHEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.]3
acaciaINACTIVE INGREDIENT5C5403N26OHEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.]3
maltodextrinINACTIVE INGREDIENT7CVR7L4A2DHEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.]3
sucraloseINACTIVE INGREDIENT96K6UQ3ZD4HEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.]3

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 28 of 33 · 654 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Premier Value Multi Symptom Antacid Berry FlavorCALCIUM CARBONATE ,MAGNESIUM HYDROXIDE,SIMETHICONEPharmacy Value Alliance LLC69e0c4a8-04ae-461b-bf47-4180bccd91d62024-10-25WarningsExact identifier
unii: H0G9379FGK
Premier Value Regular Strength Chewable Antacid Peppermint Assorted FruitANTACID TABLETSChain Drug Consortium, LLC245e195f-fd67-497b-83d4-fef75cea8b5b2024-10-25WarningsExact identifier
unii: H0G9379FGK
OHTAS ISAN ANTACIDCALCIUM CARBONATE, SODIUM BICARBONATEOHTA'S ISAN CO.,LTD.53380470-5748-6fa7-548e-7484ef204c0f2024-10-21WarningsExact identifier
unii: H0G9379FGK
OHTAS ISAN ANTACIDCALCIUM CARBONATE, SODIUM BICARBONATEOHTA'S ISAN CO.,LTD.8723fe90-8402-4511-b6c6-b71cf98513e32024-10-21WarningsExact identifier
unii: H0G9379FGK
Citrus Flavored AntacidCALCIUM CARBONATEJHK DBA American Safety & First Aid79f2b495-a438-408e-9572-b6c3516db52c2024-10-15WarningsExact identifier
unii: H0G9379FGK
NUTRALOXCALCIUM CARBONATEA-S Medication Solutions524e26a9-c69f-4e25-b83d-f4c65adca83d2024-10-11WarningsExact identifier
unii: H0G9379FGK
PrenatrylFERROUS FUMARATE, FOLIC ACIDPureTek Corporationb364551b-2ccc-4db3-e053-2995a90afbbf2024-10-08Boxed warning, Adverse reactionsExact identifier
unii: H0G9379FGK
PrenatrixFERROUS FUMARATE, FOLIC ACIDPureTek Corporationae07585b-e6e4-fd6d-e053-2995a90a7eec2024-09-30Boxed warning, Adverse reactionsExact identifier
unii: H0G9379FGK
PretrateFERROUS FUMARATE, FOLIC ACIDPureTek Corporationba4a1424-0782-77c0-e053-2a95a90a6e442024-09-30Boxed warning, Adverse reactionsExact identifier
unii: H0G9379FGK
HEB Extra Strength sugar free Antacid 174CALCIUM CARBONATEH E B17cd3717-2fc3-1693-e063-6394a90ae03d2024-09-17WarningsExact identifier
unii: H0G9379FGK
Goodsense Extra Strength AntacidCALCIUM CARBONATEGoodSense193a1805-9f57-29cd-e063-6394a90ab99f2024-09-13WarningsExact identifier
unii: H0G9379FGK
Tums Chewy BitesCALCIUM CARBONATEHaleon US Holdings LLC72ac000c-90f7-42e2-88a6-740de114a9542024-08-21WarningsExact identifier
unii: H0G9379FGK
GDC Extra strength Alkums Antacid 127AFCALCIUM CARBONATEGuardian Drug Company1b6da4a3-cfa6-6d98-e063-6394a90a58892024-08-13WarningsExact identifier
unii: H0G9379FGK
Wonderbelly Maximum Strength Antacid - Sweet MintCALCIUM CARBONATEGinger Health Company17ddf76b-237a-eeee-e063-6294a90ac2052024-07-29WarningsExact identifier
unii: H0G9379FGK
Calcium Carbonate Assorted FlavorsANTACID TABLETSNuCare Pharmaceuticals,Inc.af10dfb6-fef3-3410-e053-2995a90a91302024-07-17WarningsExact identifier
unii: H0G9379FGK
Good Neighbor Pharmacy Antacid Regular StrengthCALCIUM CARBONATEAmerisourceBergen Drug Corporation2847e82e-203e-4976-8c4f-4a5caa75ce002024-07-09WarningsExact identifier
unii: H0G9379FGK
Kirkland Ultra Stregth Antacid 171ABCALCIUM CARBONATECOSTCO WHOLESALE COMPANY1bea92e8-1b94-77b0-e063-6394a90a82122024-07-08WarningsExact identifier
unii: H0G9379FGK
Regular Strength AntacidCALCIUM CARBONATEAmerisource Bergenf9dd2797-c804-43c4-9d64-47de3b63a19a2024-06-28WarningsExact identifier
unii: H0G9379FGK
Ultra Strength Antacid Assorted FruitCALCIUM CARBONATEAmerisource Bergend39b3a19-b0e7-409d-9e0b-ef847fe8be2f2024-06-26WarningsExact identifier
unii: H0G9379FGK
Extra Strength sugar free AntacidCALCIUM CARBONATEAmerisource Bergen541a8e91-9438-4ebd-8bfc-a2674f6a9c4a2024-06-17WarningsExact identifier
unii: H0G9379FGK

Reported adverse events (FAERS/openFDA)#

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