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 | 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 | 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 | 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.
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| Signature Select Advanced Hand Sanitizer with Aloe Vera | ALCOHOL | Living Better Brands LLC | cbf0fead-0729-460b-82c0-1596c995cf2b | 2026-01-26 | Warnings | 3K9958V90M |
| Signature Select Advanced Hand Sanitizer | ALCOHOL | Living Better Brands LLC | 6d1cc25b-d612-4aae-bdb0-304758ef8f0f | 2026-01-26 | Warnings | 3K9958V90M |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.