Kiehls Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen
- Product NDC
- 49967-894
- 11-digit product format
- 499670894
- Labeler code
- 49967
- Product ID
- 49967-894_5e833585-7dc2-44a9-981e-a3cb638d1307
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate and Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- L'Oreal USA Products Inc
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-06-13
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 50; 50; 70 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| G63QQF2NOX | AVOBENZONE | 70356-09-1 | AVOBENZONE |
| V06SV4M95S | HOMOSALATE | 118-56-9 | HOMOSALATE |
| 4X49Y0596W | OCTISALATE | 118-60-5 | OCTISALATE |
| 5A68WGF6WM | OCTOCRYLENE | 6197-30-4 | OCTOCRYLENE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 49967-894-01 | 49967089401 | 125 mL in 1 BOTTLE (49967-894-01) | 125 ml | 2023-06-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | L'Oreal USA Products Inc | L'OREAL USA, INC. | 2024-06-28 | HUMAN OTC DRUG LABEL | 1 |