NDC 87330-101-12 - Daily Hydrating Mineral Body Sunscreen Broad Spectrum SPF 30 Sunscreen
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
- 87330-101
- Requested NDC
- 87330-101-12
- Package NDCs from labels
- 87330-101-11, 87330-101-12, 87330-101-13
- Manufacturer
- Oak Essentials, LLC
- Effective date
- 2026-01-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ZINC OXIDE - Oak Essentials, LLC | Oak Essentials, LLC | 2026-01-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87330-101-11 | Daily Hydrating Mineral Body SunscreenBroad Spectrum SPF 30 Sunscreen | 178 mL in 1 BOTTLE, PLASTIC | CREAM | 178 | 1 | |
| 87330-101-12 | Daily Hydrating Mineral Body SunscreenBroad Spectrum SPF 30 Sunscreen | 50 mL in 1 TUBE | CREAM | 50 | 1 | |
| 87330-101-13 | Daily Hydrating Mineral Body SunscreenBroad Spectrum SPF 30 Sunscreen | 1 in 1 BOX | CREAM | 1 | 1 |
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.