Dr.G BRIGHT TONING UP TINTED SUNSCREEN
- Product NDC
- 51621-021
- 11-digit product format
- 516210021
- Labeler code
- 51621
- Product ID
- 51621-021_30d34459-b7fc-b0c6-e063-6294a90a08ac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE, OCTISALATE, HOMOSALATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- GOWOONSESANG COSMETICS CO., LTD.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-01
- Substance
- HOMOSALATE; OCTISALATE; ZINC OXIDE
- Active strength
- 3.5; 3.5; 19.2 g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr.G BRIGHT TONING UP TINTED SUNSCREEN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HOMOSALATE | 3.5 g/100mL |
| OCTISALATE | 3.5 g/100mL |
| ZINC OXIDE | 19.2 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V06SV4M95S, 4X49Y0596W, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51621-021-01 | Dr.G BRIGHT TONING UP TINTED SUNSCREEN | 50 mL in 1 CONTAINER | CREAM | 50 | | 2 |
| 51621-021-01 | Dr.G BRIGHT TONING UP TINTED SUNSCREEN | 1 in 1 BOX | CREAM | 1 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51621-021-01 | 51621002101 | 1 CONTAINER in 1 BOX (51621-021-01) / 50 mL in 1 CONTAINER | 1 container | 2025-08-01 | No | No | Current |