NDC 56152-0253-01 - Illuminating SPF 50 plus drops Broad Spectrum Sunscreen
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
- 56152-0253
- Requested NDC
- 56152-0253-01
- Package NDCs from labels
- 56152-0253-1, 56152-0253-01
- Manufacturer
- Cosmetic Enterprise Ltd
- Effective date
- 2025-10-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Zinc Oxide - Cosmetic Enterprise Ltd | Cosmetic Enterprise Ltd | 2025-10-10 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 56152-0253-1 | Illuminating SPF 50 plus drops Broad Spectrum Sunscreen | 50 mL in 1 BOTTLE | LOTION | 50 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 56152-0253 | ILLUMINATING SPF 50 PLUS DROPS BROAD SPECTRUM SUNSCREEN (ZINC OXIDE) LOTION [COSMETIC ENTERPRISE LTD] | 1 | Current NDC, 1 package rows | 20240322_13f40485-b98e-e804-e063-6394a90af2af.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.