DAYWEAR UV WATER CREME BROAD SPECTRUM SPF 50
- Product NDC
- 11559-067
- 11-digit product format
- 115590067
- Labeler code
- 11559
- Product ID
- 11559-067_5cdf96b0-2b32-bb4a-e063-6294a90a77aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- ESTEE LAUDER INC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-02
- Substance
- HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
- Active strength
- 70; 70; 45; 30 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DAYWEAR UV WATER CREME BROAD SPECTRUM SPF 50
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| HOMOSALATE | 70 mg/mL |
| OCTOCRYLENE | 70 mg/mL |
| OCTISALATE | 45 mg/mL |
| AVOBENZONE | 30 mg/mL |
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 11559-067-01 | 11559006701 | 1 TUBE in 1 CARTON (11559-067-01) / 40 mL in 1 TUBE | 1 tube | 2026-10-02 | No | No | Current |
| 11559-067-99 | 11559006799 | 1.5 mL in 1 PACKET (11559-067-99) | 1.5 ml | 2026-10-02 | Yes | No | Current |