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