- Product NDC
- 43742-2542
- 11-digit product format
- 437422542
- Labeler code
- 43742
- Product ID
- 43742-2542_9b537207-7f9c-40c1-a81c-8ad7ba2568cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Adrenalinum, Ambra Grisea, Aurum Muriaticum Natronatum, Calcarea Sulphurica, Cimicifuga Racemosa, Cinchona Officinalis, Cortisone Aceticum, Crocus Sativus, DNA, Hyoscyamus Niger, Hypophysis Suis, Hypothalamus Suis, Ignatia Amara, Kali Bromatum, Lachesis Mutus, Pulsatilla (Pratensis), Thyroidinum (Bovine), Viola Odorata
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-03-20
- Substance
- ACONITUM NAPELLUS WHOLE; AMBERGRIS; BLACK COHOSH; CALCIUM SULFATE ANHYDROUS; CINCHONA OFFICINALIS BARK; CORTISONE ACETATE; EPINEPHRINE; HERRING SPERM DNA; HYOSCYAMUS NIGER; LACHESIS MUTA VENOM; POTASSIUM BROMIDE; PULSATILLA PRATENSIS WHOLE; SAFFRON; SODIUM TETRACHLOROAURATE; STRYCHNOS IGNATII SEED; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PITUITARY GLAND; THYROID, BOVINE; VIOLA ODORATA WHOLE
- Active strength
- 6; 6; 6; 6; 6; 8; 12; 16; 6; 12; 6; 6; 6; 15; 6; 8; 8; 8; 8 [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], Blood Coagulation Factor [EPC], Calcium [CS], Catecholamine [EPC], Catecholamines [CS], Cations, Divalent [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes