NDC 49967-161-03 - Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution
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
- 49967-161
- Requested NDC
- 49967-161-03
- Package NDCs from labels
- 49967-161-01, 49967-161-02, 49967-161-03
- Manufacturer
- L'Oreal USA Products Inc | L'OREAL USA, 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 | L'OREAL USA, INC. | 2026-01-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49967-161-01 | Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 49967-161-01 | Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution | 30 mL in 1 TUBE | CREAM | 30 | 5 | |
| 49967-161-02 | Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution | 5 mL in 1 TUBE | CREAM | 5 | 5 | |
| 49967-161-03 | Kiehls Ultra Light Daily UV Defense CC SPF 50 Anti Pollution | 3 mL in 1 PACKET | CREAM | 3 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49967-161 | KIEHLS ULTRA LIGHT DAILY UV DEFENSE CC SPF 50 ANTI POLLUTION (DROMETRIZOLE TRISILOXANE, TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, TITANIUM DIOXIDE, ETHYLHEXYL METHOXYCINNAMATE AND DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE) CREAM [L'OREAL USA PRODUCTS INC] | 4 | 4 package rows | 20231231_fc89f98e-2b9f-4abd-84ce-2200e906db03.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.