NDC 28595-715 - Altrixa
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
- 28595-715
- Package NDCs from labels
- 28595-715-30
- Manufacturer
- Allegis Pharmaceuticals, LLC
- Effective date
- 2024-03-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Altrixa - Allegis Pharmaceuticals, LLC | Allegis Pharmaceuticals, LLC | 2024-03-28 | DIETARY SUPPLEMENT |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 28595-715-30 | EA - Each | 28595-715 | 1f305694-4fd9-44e9-8426-5db53dd9e2db | 1 | 2024-05-16 |
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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| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 3 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3b21f1d8-534d-f4ea-e063-6294a90ad2eb | 2025-08-21 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 5 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3ceb3368-439c-9f6c-e063-6294a90a98ba | 2025-08-21 | Warnings | 15FIX9V2JP |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.