Home NDC 50845-0274-01 NDC 50845-0274-01 - Fem Flora Defense 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 50845-0274
Requested NDC 50845-0274-01
Package NDCs from labels 50845-0274-1, 50845-0274-01
Manufacturer Liddell Laboratories, Inc. | Apotheca Company
Effective date 2023-08-17
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50845-0274-1 Fem Flora Defense 30 mL in 1 BOTTLE, SPRAY SPRAY 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50845-0274 FEM FLORA DEFENSE (BAPTISIA TINCTORIA, BORAX, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, CINCHONA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), NITRICUM ACIDUM, PULSATILLA (PRATENSIS), PYROGENIUM, SEPIA, SULPHURICUM ACIDUM, THUJA OCCIDENTALIS) SPRAY [LIDDELL LABORATORIES, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20230818_8015e1cb-9ebd-4b3e-af57-92f2754fb790.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 68 of 225 · 4,489 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.