| Product NDC: | 68703-042 |
| Proprietary Name: | Triple Complex Diabetonic |
| Non Proprietary Name: | Calc phos, Kali sulph, Nat sulphuricum |
| Active Ingredient(s): | 6; 6; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Calc phos, Kali sulph, Nat sulphuricum |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TINCTURE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68703-042 |
| Labeler Name: | Native Remedies, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130329 |
| Package NDC: | 68703-042-60 |
| Package Description: | 59 mL in 1 BOTTLE, GLASS (68703-042-60) |
| NDC Code | 68703-042-60 |
| Proprietary Name | Triple Complex Diabetonic |
| Package Description | 59 mL in 1 BOTTLE, GLASS (68703-042-60) |
| Product NDC | 68703-042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calc phos, Kali sulph, Nat sulphuricum |
| Dosage Form Name | TINCTURE |
| Route Name | ORAL |
| Start Marketing Date | 20130329 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Native Remedies, LLC |
| Substance Name | POTASSIUM SULFATE; SODIUM SULFATE; TRIBASIC CALCIUM PHOSPHATE |
| Strength Number | 6; 6; 8 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |