- Product NDC
- 43742-0850
- 11-digit product format
- 437420850
- Labeler code
- 43742
- Product ID
- 43742-0850_25bd66ef-2437-4cc4-8ce2-b3e9a42b6992
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arsenicum Album, Berberis Vulgaris, Bryonia (Alba), Calcarea Carbonica, Carduus Marianus, Cinchona Officinalis, Kali Carbonicum, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vomica, Phosphorus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-09-15
- Substance
- ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CINCHONA OFFICINALIS BARK; LYCOPODIUM CLAVATUM SPORE; MILK THISTLE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; POTASSIUM CARBONATE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED
- Active strength
- 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes