| NDC Code | 63083-2019-2 |
|---|
| Package Description | 59 mL in 1 BOTTLE, DROPPER (63083-2019-2) |
|---|
| Product NDC | 63083-2019 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Dna Insulin Drops |
|---|
| Proprietary Name Suffix | 2019 |
|---|
| Non-Proprietary Name | Dna Insulin Drops |
|---|
| Dosage Form | LIQUID |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19840815 |
|---|
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
|---|
| Manufacturer | Professional Complementary Health Formulas |
|---|
| Substance Name | CHROMIUM; LYCOPODIUM CLAVATUM SPORE; VANADIUM; PANCRELIPASE AMYLASE; INSULIN GLULISINE; PHOSPHORIC ACID; URANYL NITRATE HEXAHYDRATE; RADIUM BROMIDE |
|---|
| Strength | 6; 6; 6; 6; 12; 30; 30; 60 |
|---|
| Strength Unit | [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
|---|
| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Insulin Analog [EPC], Insulin [Chemical/Ingredient], Standardized Chemical Allergen [EPC] |
|---|