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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
97C5T2UQ7JCHOLESTEROL57-88-5CHOLESTEROL
883WKN7W8XCORTISONE ACETATE50-04-4CORTISONE ACETATE
A4VZ22K1WTCOUMARIN91-64-5COUMARIN
YKH834O4BHEPINEPHRINE51-43-4EPINEPHRINE
V1V998DC17GARLICGARLIC
79Y1949PYOGOLD7440-57-5GOLD
VSW71SS07ILACHESIS MUTA VENOMLACHESIS MUTA VENOM
G59M7S0WS3NITROGLYCERIN55-63-0NITROGLYCERIN
H35KS68EE7POTASSIUM CHLORATE3811-04-9POTASSIUM CHLORATE
11T9HCO30OPROTEUS VULGARISPROTEUS VULGARIS
H192N84N1GRAUWOLFIA SERPENTINA8063-17-0RAUWOLFIA SERPENTINA
7114SV0MYKSELENICEREUS GRANDIFLORUS STEMSELENICEREUS GRANDIFLORUS STEM
41YPU4MMCASTRONTIUM CARBONATE1633-05-2STRONTIUM CARBONATE
70FD1KFU70SULFUR7704-34-9SULFUR
63O327782QSUS SCROFA ARTERYSUS SCROFA ARTERY
2510RH3I89SUS SCROFA VEINSUS SCROFA VEIN
QNS6W5US1ZVERATRUM ALBUM ROOTVERATRUM ALBUM ROOT

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43742-2177-14374221770130 mL in 1 BOTTLE, DROPPER (43742-2177-1) 30 ml2024-05-09NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DRUG FACTS:Deseret Biologicals, Inc. | Apotheca Company2024-05-09HUMAN OTC DRUG LABEL1