Ultra Sunscreen
- Product NDC
- 85448-003
- 11-digit product format
- 854480003
- Labeler code
- 85448
- Product ID
- 85448-003_4ed974b8-6c12-08e0-e063-6294a90a7713
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Titanium Dioxide
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- Jiangsu Senwo Medical Technology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-07
- Substance
- OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
- Active strength
- .09; .035; .027 g/mL; g/mL; g/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ultra Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | .09 g/mL |
| OCTISALATE | .035 g/mL |
| TITANIUM DIOXIDE | .027 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, 4X49Y0596W, 15FIX9V2JP |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85448-003-01 | Ultra Sunscreen | 473 mL in 1 BOTTLE | EMULSION | 473 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85448-003-01 | 85448000301 | 473 mL in 1 BOTTLE (85448-003-01) | 473 ml | 2026-04-07 | No | No | Historical |