NDC 52747-306 - Hemocyte F
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
- 52747-306
- Package NDCs from labels
- 52747-306-70, 52747-306-30
- Manufacturer
- US Pharmaceutical Corporation | PD SUB, LLC.
- Effective date
- 2014-10-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hemocyte F | US Pharmaceutical Corporation | PD SUB, LLC. | 2014-10-10 | Dietary Supplement |
| Hemocyte F | US Pharmaceutical Corporation | PD SUB, LLC. | 2014-10-10 | Dietary Supplement |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52747-306-30 | EA - Each | 52747-306 | 93b2847a-c63f-4b92-bf68-01ac230043bf | 1 | 2014-11-05 |
| 52747-306-70 | EA - Each | 52747-306 | b21cba32-ddc0-4bee-b125-820a4fcf79ea | 1 | 2014-11-05 |
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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| SPF 50 MINERAL SUNSCREEN LIP | ZINC OXIDE , TITANIUM DIOXIDE | Guangzhou Tata Biotechnology Co., Ltd. | 1c6f0964-9bee-1c06-e063-6294a90ac2a4 | 2025-12-22 | Warnings | 15FIX9V2JP |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.