NDC11 10210005701
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 10210-0057-01 | 10210-0057 |
| 10210-0057-1 | 10210-0057 |
| 10210-057-01 | 10210-057 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Carmex 10 Count Variety Pack SPF 15 Sunscreen | OCTINOXATE, OXYBENZONE, PETROLATUM | Carma Laboratories, Inc. | bacc60ec-0b6a-4ba2-b246-a59694f06b77 | 2023-10-25 | Warnings | 10210-0057-1 10210-0057 10210005701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.