- Product NDC
- 43406-0611
- 11-digit product format
- 434060611
- Labeler code
- 43406
- Product ID
- 43406-0611_c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Borate, Oyster Shell Calcium Carbonate Crude, Calcium Fluoride, Tribasic Calcium Phosphate, Eupatorium Perfoliatum Flowering Top, Iron, Hydrofluoric Acid, Hekla Lava, Toxicodendron Pubescens Leaf, Ruta Graveolens Flowering Top, Silicon Dioxide, Comfrey Root.
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Natural Creations, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-06-01
- Substance
- CALCIUM FLUORIDE; COMFREY ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; HEKLA LAVA; HYDROFLUORIC ACID; IRON; OYSTER SHELL CALCIUM CARBONATE, CRUDE; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE; SODIUM BORATE; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATE
- Active strength
- 30; 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; [hp_C]/mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes