Home NDC 82969-2159-01 NDC 82969-2159-01 - Bestmade Natural Products BM159 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 82969-2159
Requested NDC 82969-2159-01
Package NDCs from labels 82969-2159-1, 82969-2159-01
Manufacturer Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
Effective date 2025-02-18
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type BM159 Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro 2025-02-18 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82969-2159-1 Bestmade Natural Products BM159 30 [hp_C] in 1 BOTTLE, GLASS LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82969-2159 BESTMADE NATURAL PRODUCTS BM159 (ALETRIS FARINOSA, ASHOKA JANO, FLUORIC ACID, FUMARIC ACID, HYDRASTIS, HYDROCOTYLE ASIATICA, KALI BICH, KREASOTE) LIQUID [BESTMADE NATURAL PRODUCTS] 1 Current NDC, 1 package rows 20250417_2e6c7481-b1cb-e3a6-e063-6294a90af087.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 82 of 180 · 3,585 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.