Reboost
- Product NDC
- 50114-8550
- 11-digit product format
- 501148550
- Labeler code
- 50114
- Product ID
- 50114-8550_ba1d7b8e-0475-40f3-9fef-5b20fb600ec0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANTIMONY POTASSIUM TARTRATE
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Heel Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-02-13
- Marketing end
- 0000-00-00
- Substance
- ANTIMONY POTASSIUM TARTRATE; CUPRIC SULFATE; DROSERA ROTUNDIFOLIA; IPECAC; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED
- Active strength
- 6 [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50114-8550-1 | Reboost | 1 in 1 CARTON | SYRUP | 1 | | 1 |
| 50114-8550-1 | Reboost | 125 mL in 1 BOTTLE | SYRUP | 125 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50114-8550 | REBOOST (ANTIMONY POTASSIUM TARTRATE) SYRUP [HEEL INC] | 1 | Legacy NDC, 2 package rows | 20130214_0ed2766d-df0b-40c9-82e4-aee35cc0332c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50114-8550-1 | 50114855001 | 1 in 1 CARTON | Historical |