- Product NDC
- 71954-729
- 11-digit product format
- 719540729
- Labeler code
- 71954
- Product ID
- 71954-729_d44c8873-88ab-30c5-e053-2995a90a5170
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aceticum Acidum, Anacardium Orientale, Baryta Iodata, Calcarea Carbonica, Capsicum Annum, Fucus Vesiculosus, Graphites, Natrum Sulphuricum, Phytolacca Decandra, Stannum Metallicum, Thyrdoidinum, Zinum Metallicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- WELL BODY CONCEPTS LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-05-01
- Substance
- ACETIC ACID; BARIUM IODIDE; CAPSICUM; FUCUS VESICULOSUS; GRAPHITE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; SEMECARPUS ANACARDIUM JUICE; SODIUM SULFATE; THYROID, UNSPECIFIED; TIN; ZINC
- Active strength
- 10; 12; 12; 5; 12; 12; 7; 12; 12; 12; 12; 12 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes