BP Reg
- Product NDC
- 43742-2177
- 11-digit product format
- 437422177
- Labeler code
- 43742
- Product ID
- 43742-2177_fc50a508-522c-45e0-8ef7-0d6c684e88ff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adrenalinum, Allium Sativum, Alpha-Lipoicum Acidum, Arteria Suis, Aurum Metallicum, Cactus Grandiflorus, Cholesterinum, Cortisone Aceticum, Coumarinum, Formalinum, Glonoinum, Kali Chloricum, Lachesis Mutus, Proteus (Vulgaris), Rauwolfia Serpentina, Strontium Carbonicum, Sulphur, Thyroidinum (Suis), Vena Suis, Veratrum Album
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-05-09
- Substance
- ALPHA LIPOIC ACID; CHOLESTEROL; CORTISONE ACETATE; COUMARIN; EPINEPHRINE; FORMALDEHYDE SOLUTION; GARLIC; GOLD; LACHESIS MUTA VENOM; NITROGLYCERIN; POTASSIUM CHLORATE; PROTEUS VULGARIS; RAUWOLFIA SERPENTINA; SELENICEREUS GRANDIFLORUS STEM; STRONTIUM CARBONATE; SULFUR; SUS SCROFA ARTERY; SUS SCROFA VEIN; THYROID; VERATRUM ALBUM ROOT
- Active strength
- 12; 12; 8; 12; 8; 9; 6; 12; 12; 12; 9; 16; 12; 12; 12; 12; 8; 8; 8; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Vasodilation [PE], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BP Reg
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| EPINEPHRINE | 12 [hp_X]/mL |
| GARLIC | 12 [hp_X]/mL |
| ALPHA LIPOIC ACID | 8 [hp_X]/mL |
| SUS SCROFA ARTERY | 12 [hp_X]/mL |
| GOLD | 8 [hp_X]/mL |
| SELENICEREUS GRANDIFLORUS STEM | 9 [hp_X]/mL |
| CHOLESTEROL | 6 [hp_X]/mL |
| CORTISONE ACETATE | 12 [hp_X]/mL |
| COUMARIN | 12 [hp_X]/mL |
| FORMALDEHYDE SOLUTION | 12 [hp_X]/mL |
| NITROGLYCERIN | 9 [hp_X]/mL |
| POTASSIUM CHLORATE | 16 [hp_X]/mL |
| LACHESIS MUTA VENOM | 12 [hp_X]/mL |
| PROTEUS VULGARIS | 12 [hp_X]/mL |
| RAUWOLFIA SERPENTINA | 12 [hp_X]/mL |
| STRONTIUM CARBONATE | 12 [hp_X]/mL |
| SULFUR | 8 [hp_X]/mL |
| THYROID | 8 [hp_X]/mL |
| SUS SCROFA VEIN | 8 [hp_X]/mL |
| VERATRUM ALBUM ROOT | 12 [hp_X]/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| YKH834O4BH | Internal UNII lookup |
| V1V998DC17 | Internal UNII lookup |
| 73Y7P0K73Y | Internal UNII lookup |
| 63O327782Q | Internal UNII lookup |
| 79Y1949PYO | Internal UNII lookup |
| 7114SV0MYK | Internal UNII lookup |
| 97C5T2UQ7J | Internal UNII lookup |
| 883WKN7W8X | Internal UNII lookup |
| A4VZ22K1WT | Internal UNII lookup |
| T0H3L6C7I5 | Internal UNII lookup |
| G59M7S0WS3 | Internal UNII lookup |
| H35KS68EE7 | Internal UNII lookup |
| VSW71SS07I | Internal UNII lookup |
| 11T9HCO30O | Internal UNII lookup |
| H192N84N1G | Internal UNII lookup |
| 41YPU4MMCA | Internal UNII lookup |
| 70FD1KFU70 | Internal UNII lookup |
| 6RV024OAUQ | Internal UNII lookup |
| 2510RH3I89 | Internal UNII lookup |
| QNS6W5US1Z | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 540c1149-b6d4-4926-87e8-73a920f87b4a | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43742-2177-1 | BP Reg | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43742-2177 | BP REG (ADRENALINUM, ALLIUM SATIVUM, ALPHA-LIPOICUM ACIDUM, ARTERIA SUIS, AURUM METALLICUM, CACTUS GRANDIFLORUS, CHOLESTERINUM, CORTISONE ACETICUM, COUMARINUM, FORMALINUM, GLONOINUM, KALI CHLORICUM, LACHESIS MUTUS, PROTEUS (VULGARIS), RAUWOLFIA SERPENTINA, STRONTIUM CARBONICUM, SULPHUR, THYROIDINUM (SUIS), VENA SUIS, VERATRUM ALBUM) LIQUID [DESERET BIOLOGICALS, INC.] | 1 | Current NDC, 1 package rows | 20240514_540c1149-b6d4-4926-87e8-73a920f87b4a.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| BP Reg | ADRENALINUM, ALLIUM SATIVUM, ALPHA-LIPOICUM ACIDUM, ARTERIA SUIS, AURUM METALLICUM, CACTUS GRANDIFLORUS, CHOLESTERINUM, CORTISONE ACETICUM, COUMARINUM, FORMALINUM, GLONOINUM, KALI CHLORICUM, LACHESIS MUTUS, PROTEUS (VULGARIS), RAUWOLFIA SERPENTINA, STRONTIUM CARBONICUM, SULPHUR, THYROIDINUM (SUIS), VENA SUIS, VERATRUM ALBUM | Deseret Biologicals, Inc. | 540c1149-b6d4-4926-87e8-73a920f87b4a | 2024-05-09 | Warnings | 43742-2177 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 43742-2177-1 | 43742217701 | 30 mL in 1 BOTTLE, DROPPER (43742-2177-1) | 30 ml | 2024-05-09 | No | No | Current |