Product NDC: | 57955-5070 |
Proprietary Name: | Bone Strengthener |
Non Proprietary Name: | Calcarea carbonica, Calcarea fluorica, Calcarea phosphorica, Equisetum hyemale, Hekla lava, Phosphorus, and silicea |
Active Ingredient(s): | 10; 10; 10; 10; 10; 10; 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL & nbsp; Calcarea carbonica, Calcarea fluorica, Calcarea phosphorica, Equisetum hyemale, Hekla lava, Phosphorus, and silicea |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57955-5070 |
Labeler Name: | King Bio Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120130 |
Package NDC: | 57955-5070-2 |
Package Description: | 59 mL in 1 BOTTLE, SPRAY (57955-5070-2) |
NDC Code | 57955-5070-2 |
Proprietary Name | Bone Strengthener |
Package Description | 59 mL in 1 BOTTLE, SPRAY (57955-5070-2) |
Product NDC | 57955-5070 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Calcarea carbonica, Calcarea fluorica, Calcarea phosphorica, Equisetum hyemale, Hekla lava, Phosphorus, and silicea |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120130 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | King Bio Inc. |
Substance Name | CALCIUM FLUORIDE; EQUISETUM HYEMALE; HEKLA LAVA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SILICON DIOXIDE; TRIBASIC CALCIUM PHOSPHATE |
Strength Number | 10; 10; 10; 10; 10; 10; 10 |
Strength Unit | [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
Pharmaceutical Classes |