NDC 68026-821 - La Prairie Concealer-Foundation Sunscreen SPF 15 PETALE
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
- 68026-821
- Package NDCs from labels
- 68026-821-30
- Manufacturer
- La Prairie, Inc.
- Effective date
- 2025-02-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| La Prairie Concealer-Foundation Sunscreen SPF 15 - PETALE | La Prairie, Inc. | 2025-02-21 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68026-821-30 | La Prairie Concealer-Foundation Sunscreen SPF 15 PETALE | 1 in 1 BOX | CREAM | 60 mg in 1mL | 4 | |
| 68026-821-30 | La Prairie Concealer-Foundation Sunscreen SPF 15 PETALE | 30 mL in 1 BOTTLE | CREAM | 30 mL | 60 mg in 1mL | 4 |
DailyMed Dashboard NDC Coverage#
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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|---|---|---|---|---|---|---|
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| Aquaphor Healing | PETROLATUM | Beiersdorf Inc | 0a17bf6f-6114-4647-a509-65999255c37b | 2025-12-15 | Warnings | 4T6H12BN9U |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.