NDC11 64024094909
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 |
|---|---|
| 64024-0949-09 | 64024-0949 |
| 64024-0949-9 | 64024-0949 |
| 64024-949-09 | 64024-949 |
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 |
|---|---|---|---|---|---|---|
| Aldi LACURA Ultra Light Dry-Touch 100 Sunscreen | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE | ALDI INC | f7b2cf4e-468c-3406-e053-6394a90a2139 | 2024-10-21 | Warnings | 64024-949-09 64024-949 64024094909 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.