NDC 51531-0294 - MK Men Advanced Facial Hydrator Sunscreen SPF 30
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
- 51531-0294
- Package NDCs from labels
- 51531-0294-3
- Manufacturer
- Mary Kay Inc.
- Effective date
- 2020-08-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MK Men SPF 30 Sunscreen EU Export Only | Mary Kay Inc. | 2020-08-24 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51531-0294-3 | MK Men Advanced Facial Hydrator Sunscreen SPF 30 | 1 in 1 CARTON | LOTION | 1 | 3 | |
| 51531-0294-3 | MK Men Advanced Facial Hydrator Sunscreen SPF 30 | 88 mL in 1 TUBE | LOTION | 88 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51531-0294 | MK MEN ADVANCED FACIAL HYDRATOR SUNSCREEN SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [MARY KAY INC.] | 3 | 2 package rows | 20200825_d12223bd-5eae-411b-8bdb-814b0e61a240.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.