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 |