NDC 49967-397 - Garnier Ombrelle Complete Sensitive Advanced Lightweight hypoallergenic SPF 45 Mexoryl Technology
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
- 49967-397
- Package NDCs from labels
- 49967-397-01, 49967-397-02
- Manufacturer
- L'Oreal USA Products Inc | L'OREAL USA PRODUCTS, INC.
- Effective date
- 2025-12-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | L'Oreal USA Products Inc | L'OREAL USA PRODUCTS, INC. | 2025-12-09 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49967-397-01 | Garnier Ombrelle Complete Sensitive Advanced Lightweight hypoallergenic SPF 45 Mexoryl Technology | 1 in 1 CARTON | LOTION | 1 | 4 | |
| 49967-397-01 | Garnier Ombrelle Complete Sensitive Advanced Lightweight hypoallergenic SPF 45 Mexoryl Technology | 90 mL in 1 TUBE | LOTION | 90 | 4 | |
| 49967-397-02 | Garnier Ombrelle Complete Sensitive Advanced Lightweight hypoallergenic SPF 45 Mexoryl Technology | 1 in 1 CARTON | LOTION | 1 | 4 | |
| 49967-397-02 | Garnier Ombrelle Complete Sensitive Advanced Lightweight hypoallergenic SPF 45 Mexoryl Technology | 200 mL in 1 TUBE | LOTION | 200 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49967-397 | GARNIER OMBRELLE COMPLETE SENSITIVE ADVANCED LIGHTWEIGHT HYPOALLERGENIC SPF 45 MEXORYL TECHNOLOGY (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE AND DROMETRIZOLE TRISILOXANE) LOTION [L'OREAL USA PRODUCTS INC] | 3 | 4 package rows | 20240101_f34fcf82-9b85-4ff8-8e80-fa92f9c5a606.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.