Home NDC 51596-005-01 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 Label Manufacturer Effective date Type Heartburn Relief to Go ™ Breakthrough Products Inc. 2014-10-06 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51596-005-01 Heartburn Relief to Go 1 in 1 POUCH POWDER 1 3 51596-005-05 Heartburn Relief to Go 5 in 1 BOX POWDER 5 3 51596-005-10 Heartburn Relief to Go 1 in 1 PACKET POWDER 1 3 51596-005-10 Heartburn Relief to Go 10 in 1 BOX POWDER 10 3 51596-005-12 Heartburn Relief to Go 12 in 1 BOX POWDER 12 3 51596-005-24 Heartburn Relief to Go 24 in 1 BOX POWDER 24 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51596-005 HEARTBURN RELIEF TO GO (CALCIUM CARBONATE) POWDER [BREAKTHROUGH PRODUCTS INC.] 3 Legacy NDC, 6 package rows 20141017_88cadd90-c6f4-4229-aed4-bf3e4ce6dbf5.zip
DailyMed Socrata Ingredients# 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 33 of 33 · 654 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.