NDC 82969-6002-01 - Bestmade Natural Products Field of Flowers Formula
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
- 82969-6002
- Requested NDC
- 82969-6002-01
- Package NDCs from labels
- 82969-6002-1, 82969-6002-01
- Manufacturer
- Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro
- Effective date
- 2025-03-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Field of flowers formula | Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro | 2025-03-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82969-6002-1 | Bestmade Natural Products Field of Flowers Formula | 6 [hp_X] in 1 BOTTLE, GLASS | LIQUID | 6 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 82969-6002 | BESTMADE NATURAL PRODUCTS FIELD OF FLOWERS FORMULA (AESCULUS CAR, AESCULUS HIP, AGRIMONIA EUP, BROMUS RAM, CALLUNA VULG, CARPINUS BET, CASTANEA SAT, CENTAURIUM UMB, CERATOSTIGMA WILLM, CICHORIUM INT, CLEMATIS VIT, FAGUS SYLV, GENTIANELLA AMARELLA, HELIANTHEMUM NUMMULARIUM, ILEX AQUIFOLIUM, IMPATIENS GLAND, LARIX DECIDUA, LONICERA CAPRIFOLIUM, MALUS, MIMULUS GUT, OLEA EUROP, ORNITHOGALUM UMB, PINUS SYL, POPULUS TREM, PRUNUS CERA, QUERCUS ROB, ROCK WATER, ROSA CAN, SALIX VIT, SCLERANTHUS ANNNUS, SINAPIS ARV, ULEX EURO, ULMUS PROC, VERBENA, VITIS VIN) LIQUID [BESTMADE NATURAL PRODUCTS] | 1 | Current NDC, 1 package rows | 20250326_2fbf9b7c-e54f-589d-e063-6394a90a14a7.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.