Bestmade Natural Products BM103
- Product NDC
- 82969-2103
- 11-digit product format
- 829692103
- Labeler code
- 82969
- Product ID
- 82969-2103_2d8ad86f-b2f2-8b91-e063-6294a90a641c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Bichromicum, Nitricum Acidum, Graphites, Phosphorus, Hydrastis, Condurango, Ornithogalum, Uran. Nit, Nat Phos
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Bestmade Natural Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- GOLDENSEAL; GRAPHITE; NITRIC ACID; ORNITHOGALUM UMBELLATUM; PHOSPHORUS; POTASSIUM DICHROMATE; RUEHSSIA CUNDURANGO BARK; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; URANYL NITRATE HEXAHYDRATE
- Active strength
- 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| ZW3Z11D0JV | GOLDENSEAL | | GOLDENSEAL |
| 4QQN74LH4O | GRAPHITE | 7782-42-5 | GRAPHITE |
| 411VRN1TV4 | NITRIC ACID | 7697-37-2 | NITRIC ACID |
| 9NS3M2Y78S | ORNITHOGALUM UMBELLATUM | | ORNITHOGALUM UMBELLATUM |
| 27YLU75U4W | PHOSPHORUS | 7723-14-0 | PHOSPHORUS |
| T4423S18FM | POTASSIUM DICHROMATE | 7778-50-9 | POTASSIUM DICHROMATE |
| 70WT22SF4B | SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE | 7782-85-6 | SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE |
| 3V057702FY | URANYL NITRATE HEXAHYDRATE | 13520-83-7 | URANYL NITRATE HEXAHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82969-2103-1 | 82969210301 | 30 [hp_C] in 1 BOTTLE, GLASS (82969-2103-1) | 2015-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| BM103 | Bestmade Natural Products | Total Operations Management LLC DBA: Bestmade Natural Products Micro | 2025-02-07 | HUMAN OTC DRUG LABEL | 1 |