D-12 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Potassium Iodide; Calcium Iodide; Arsenic Triiodide; Barium Chloride Dihydrate; Nitroglycerin; Conium Maculatum Flowering Top; Arnica Montana; Phosphorus; Gold Trichloride.
| Product ID | 58264-0012_b4621248-7d08-45ff-aace-873016078b91 | 
| NDC | 58264-0012 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | D-12 | 
| Generic Name | Potassium Iodide, Calcium Iodide, Arsenic Triiodide, Barium Chloride Dihydrate, Nitroglycerin, Conium Maculatum Flowering Top, Arnica Montana, Phosphorus, And Gold Trichloride | 
| Dosage Form | Solution | 
| Route of Administration | SUBLINGUAL | 
| Marketing Start Date | 1990-01-01 | 
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC | 
| Labeler Name | DNA Labs, Inc. | 
| Substance Name | POTASSIUM IODIDE; CALCIUM IODIDE; ARSENIC TRIIODIDE; BARIUM CHLORIDE DIHYDRATE; NITROGLYCERIN; CONIUM MACULATUM FLOWERING TOP; ARNICA MONTANA; PHOSPHORUS; GOLD TRICHLORIDE | 
| Active Ingredient Strength | 3 [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 | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 1990-01-01 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | Unapproved homeopathic | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 1990-01-01 | 
| Inactivation Date | 2020-01-31 | 
| Ingredient | Strength | 
|---|---|
| POTASSIUM IODIDE | 3 [hp_X]/mL | 
| SPL SET ID: | cd69e429-32af-4d77-9ec1-c40cfc7fe414 | 
| Manufacturer | |
| UNII | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  D-12  73333407  not registered Dead/Abandoned | MICOBRA CORPORATION, THE 0000-00-00 |