NDC 82969-2173-01 - Bestmade Natural Products BM173
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
- 82969-2173
- Requested NDC
- 82969-2173-01
- Package NDCs from labels
- 82969-2173-1, 82969-2173-01
- Manufacturer
- Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
- Effective date
- 2025-02-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BM173 | Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro | 2025-02-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82969-2173-1 | Bestmade Natural Products BM173 | 30 [hp_C] in 1 BOTTLE, GLASS | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 82969-2173 | BESTMADE NATURAL PRODUCTS BM173 (ECHINACEA, EUPHRASIA, NATRUM MUR, RHUS TOX, SILICEA, SULPHUR, URTICA UREN) LIQUID [BESTMADE NATURAL PRODUCTS] | 1 | Current NDC, 1 package rows | 20250416_2e7de086-a4c1-ae9e-e063-6394a90aa5f5.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.
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| Cold Crush Adult | ACONITUM NAPELLUS, ALLIUM CEPA, BRYONIA ALBA, EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, NUX VOMICA, PULSATILLA, RHUS TOXICODENDRON, SABADILLA | Genexa Inc. | 78ff93d3-5c77-b951-e053-2a91aa0adda9 | 2026-08-22 | Warnings | C9642I91WL |
| Genexa Kids Allergy Care | ALLIUM CEPA, DULCAMARA, EUPHRASIA OFFICINALIS, NUX VOMICA, PULSATILLA, ROSA DAMASCENA, SABIDILLA, SINAPIS NIGRA, WYETHIA HELENOIDES | Genexa Inc. | ba0da07a-107b-2c66-e053-2995a90ab96a | 2026-08-22 | Warnings | C9642I91WL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.