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Reboost
Reboost - 50114-8550-1 - (ANTIMONY POTASSIUM TARTRATE)
Drug Information of Reboost
| Product NDC: | 50114-8550 |
| Proprietary Name: | Reboost |
| Non Proprietary Name: | ANTIMONY POTASSIUM TARTRATE |
| Active Ingredient(s): | 6; 6; 4; 4; 4; 8 [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL & nbsp; ANTIMONY POTASSIUM TARTRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Reboost
| Product NDC: | 50114-8550 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130213 |
Package Information of Reboost
| Package NDC: | 50114-8550-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (50114-8550-1) > 125 mL in 1 BOTTLE |
NDC Information of Reboost
| NDC Code | 50114-8550-1 |
| Proprietary Name | Reboost |
| Package Description | 1 BOTTLE in 1 CARTON (50114-8550-1) > 125 mL in 1 BOTTLE |
| Product NDC | 50114-8550 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ANTIMONY POTASSIUM TARTRATE |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20130213 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | ANTIMONY POTASSIUM TARTRATE; CUPRIC SULFATE; DROSERA ROTUNDIFOLIA; IPECAC; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED |
| Strength Number | 6; 6; 4; 4; 4; 8 |
| Strength Unit | [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL |
| Pharmaceutical Classes |
