Home NDC 0280-0272 NDC 0280-0272 - Calcemin Advance 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 0280-0272
Package NDCs from labels 0280-0272-30, 0280-0272-60, 0280-0272-12
Manufacturer Bayer HealthCare LLC.
Effective date 2025-09-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Calcemin Advance Bayer HealthCare LLC. 2025-09-16 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 0280-0272-12 Calcemin Advance 1 in 1 CARTON TABLET, FILM COATED 1 5 0280-0272-12 Calcemin Advance 120 in 1 BOTTLE TABLET, FILM COATED 120 5 0280-0272-30 Calcemin Advance 1 in 1 CARTON TABLET, FILM COATED 1 5 0280-0272-30 Calcemin Advance 30 in 1 BOTTLE TABLET, FILM COATED 30 5 0280-0272-60 Calcemin Advance 60 in 1 BOTTLE TABLET, FILM COATED 60 5 0280-0272-60 Calcemin Advance 1 in 1 CARTON TABLET, FILM COATED 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0280-0272 CALCEMIN ADVANCE (CALCIUM CITRATE) TABLET, FILM COATED [BAYER HEALTHCARE LLC.] 3 6 package rows 20200529_3161469e-6402-607a-e054-00144ff88e88.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 43 of 290 · 5,793 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.