NDC 50107-200 - Reme-Flu
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50107-200
- Package NDCs from labels
- 50107-200-00
- Manufacturer
- Legacy Biotechnologies Inc. | Washington Homeopathic Products
- Effective date
- 2009-12-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Reme-Flu - Legacy Biotechnologies Inc. | Washington Homeopathic Products | Legacy Biotechnologies Inc. | Washington Homeopathic Products | 2009-12-22 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50107-200-00 | Reme-Flu | 12 in 1 BOTTLE, DROPPER | LIQUID | 12 | 3 [hp_X] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50107-200 | REME-FLU (BRYONIA ALBA ROOT,EUPATORIUM PERFOLIATUM FLOWERING TOP,GELSEMIUM SEMPERVIRENS ROOT, ARSENIC, ERIODICTYON, EUCALYPTUS GLOBULUS LEAF , INULA, SAMBUCUS NIGRA FLOWER, POTASSIUM CHLORIDE, SODIUM CHLORIDE , MAGNESIUM PHOSPHATE , TRIBASIC CALCIUM PHOSPHATE ) KIT [LEGACY BIOTECHNOLOGIES INC.] | 1 | Unmatched | 20091224_705f016c-4bdc-4a5c-8b38-324eee861cf2.zip |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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| PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam | ALCOHOL | GOJO Industries, Inc. | 4fa85619-257f-4a19-a8f2-5a2e4b809726 | 2024-12-11 | Warnings | 3K9958V90M |
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| CVS Hand Sanitizer | ALCOHOL | CVS | b5faeb31-67c7-2000-e053-2995a90a1409 | 2024-12-10 | Warnings | 3K9958V90M |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.