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 |