Reboost (Heel Inc)
Welcome to the PulseAid listing for the Reboost drug offered from Heel Inc. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Heel Inc |
| NON-PROPRIETARY NAME: | ANTIMONY POTASSIUM TARTRATE |
| SUBSTANCE NAME: | ANTIMONY POTASSIUM TARTRATE; CUPRIC SULFATE; DROSERA ROTUNDIFOLIA; IPECAC; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | SYRUP |
| MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
| START MARKETING DATE: | 2013-02-13 |
| END MARKETING DATE: | 0000-00-00 |
Reboost HUMAN OTC DRUG Details:
| Item Description | Reboost from Heel Inc |
| LABELER NAME: | Heel Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 6; 6; 4; 4; 4; 8([hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL) |
| START MARKETING DATE: | 2013-02-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50114-8550_ba1d7b8e-0475-40f3-9fef-5b20fb600ec0 |
| PRODUCT NDC: | 50114-8550 |
| APPLICATION NUMBER: | |
Other ANTIMONY POTASSIUM TARTRATE; CUPRIC SULFATE; DROSERA ROTUNDIFOLIA; IPECAC; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED Pharmaceutical Manufacturers / Labelers:
