Sun Zapper - Pure Zinc Sunscreen SPF50
- Product NDC
- 83252-121
- 11-digit product format
- 832520121
- Labeler code
- 83252
- Product ID
- 83252-121_5d399fda-e5df-a728-e063-6294a90a8baa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Veganic SKN Limited
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-20
- Substance
- ZINC OXIDE
- Active strength
- 25 kg/100kg
- 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
- Sun Zapper - Pure Zinc Sunscreen SPF50
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC OXIDE | 25 kg/100kg |
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 | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 83252-121-03 | 83252012103 | .1 kg in 1 TUBE (83252-121-03) | 2026-10-07 | No | No | Current |
| 83252-121-17 | 83252012117 | .24 kg in 1 TUBE (83252-121-17) | 2026-10-07 | No | No | Current |
| 83252-121-25 | 83252012125 | .1 kg in 1 BOTTLE, PUMP (83252-121-25) | 2025-08-20 | No | No | Current |