Sunsei SPF 30 Sunscreen
- Product NDC
- 85791-3031
- 11-digit product format
- 857913031
- Labeler code
- 85791
- Product ID
- 85791-3031_4c9ff572-3664-8d8f-e063-6294a90abde7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shimoda Prime Products, LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-15
- Substance
- ZINC OXIDE
- Active strength
- 20 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunsei SPF 30 Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 20 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85791-3031-1 | Sunsei SPF 30 Sunscreen | 89 mL in 1 TUBE | LIQUID | 89 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85791-3031-1 | 85791303101 | 89 mL in 1 TUBE (85791-3031-1) | 89 ml | 2026-03-15 | No | No | Historical |