NDC 69846-502 - LYDIA PINKHAM Herbal Supplement
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
- 69846-502
- Manufacturer
- NUMARK BRANDS, INC | INTERNATIONAL FRUTAROM CORP
- Effective date
- 2016-08-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ascorbic Acid - NUMARK BRANDS, INC | INTERNATIONAL FRUTAROM CORP | NUMARK BRANDS, INC | INTERNATIONAL FRUTAROM CORP | 2016-08-12 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 038485502085 | LYDIA PINKHAM Herbal Supplement | 1 in 1 CARTON | LIQUID | 1 | 1 | |
| 038485502085 | LYDIA PINKHAM Herbal Supplement | 8 mL in 1 BOTTLE | LIQUID | 8 | 1 | |
| 038485502160 | LYDIA PINKHAM Herbal Supplement | 1 in 1 CARTON | LIQUID | 1 | 1 | |
| 038485502160 | LYDIA PINKHAM Herbal Supplement | 473 mL in 1 BOTTLE | LIQUID | 473 | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.