Mineral Sunscreen SPF 50
- Product NDC
- 70631-137
- 11-digit product format
- 706310137
- Labeler code
- 70631
- Product ID
- 70631-137_2b377557-c2de-ba26-e063-6394a90a64ad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Young Living Essential Oils, LC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-07-23
- Substance
- ZINC OXIDE
- Active strength
- 22 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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
- Mineral Sunscreen SPF 50
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC OXIDE | 22 g/100g |
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 | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70631-137-85 | 70631013785 | 85 g in 1 TUBE (70631-137-85) | 85 g | 2021-07-23 | 0000-00-00 | No | No | Current |