Fountain of Youth Mineral SPF 30 Sunscreen
- Product NDC
- 87593-105
- 11-digit product format
- 875930105
- Labeler code
- 87593
- Product ID
- 87593-105_5d786f6a-f11b-04de-e063-6394a90ac584
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fountain of Youth Mineral SPF 30 Sunscreen
- Dosage form
- LOTION
- Route
- CUTANEOUS
- Labeler
- Lance (Guangzhou) Biological Technology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-07-13
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 12; 3.6 g/120g; g/120g
- 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
- Fountain of Youth Mineral SPF 30 Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC OXIDE | 12 g/120g |
| TITANIUM DIOXIDE | 3.6 g/120g |
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 |
|---|---|---|---|---|---|---|---|
| 87593-105-04 | 87593010504 | 120 g in 1 TUBE (87593-105-04) | 120 g | 2026-07-13 | No | No | Current |