Sunright 50
- Product NDC
- 62839-2011
- 11-digit product format
- 628392011
- Labeler code
- 62839
- Product ID
- 62839-2011_b43a24fc-7faa-4721-9f72-7fc5b4fd857c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, and Octinoxate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- NSE Products, Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-05-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTINOXATE
- Active strength
- 30; 150; 50 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunright 50
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/mL |
| HOMOSALATE | 150 mg/mL |
| OCTINOXATE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4Y5P7MUD51 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62839-2011-1 | Sunright 50 | 100 mL in 1 TUBE | LOTION | 100 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62839-2011-1 | 62839201101 | 100 mL in 1 TUBE (62839-2011-1) | 100 ml | 2021-05-01 | No | No | Current |