NDC 49967-123 - Kiehls Activated Sun Protector Sunscreen SPF 50 For Face and Body For All Skin Types
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
- 49967-123
- Package NDCs from labels
- 49967-123-01, 49967-123-02
- Manufacturer
- L'Oreal USA Products Inc | Cosmetic Essence, LLC | Universal Packaging Systems, Inc.
- Effective date
- 2026-01-07
- 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 | Cosmetic Essence, LLC | Universal Packaging Systems, Inc. | 2026-01-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49967-123-01 | Kiehls Activated Sun Protector Sunscreen SPF 50 For Face and Body For All Skin Types | 150 mL in 1 TUBE | LOTION | 150 | 7 | |
| 49967-123-02 | Kiehls Activated Sun Protector Sunscreen SPF 50 For Face and Body For All Skin Types | 5 mL in 1 PACKET | LOTION | 5 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49967-123 | KIEHLS ACTIVATED SUN PROTECTOR SUNSCREEN SPF 50 FOR FACE AND BODY FOR ALL SKIN TYPES (ETHYLHEXYL TRIAZONE, DROMETRIZOLE TRISILOXANE, HOMOSALATE, TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID, ETHYLHEXYL SALICYLATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE AND DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE) LOTION [L'OREAL USA PRODUCTS INC] | 6 | 2 package rows | 20241228_cb0944e9-072d-4ef7-8b12-de3da6cf96be.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.