NDC11 00299493002
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 |
|---|---|
| 00299-4930-02 | 00299-4930 |
| 00299-4930-2 | 00299-4930 |
| 0299-4930-02 | 0299-4930 |
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 |
|---|---|---|---|---|---|---|
| Cetaphil Daily Facial Moisturizer with suncreen SPF 50 | OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE | Galderma Laboratories, L.P. | 6650d137-e69e-4ec2-8311-3de74bf21315 | 2024-04-17 | Warnings | 0299-4930-02 0299-4930 00299493002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.