SUNSCREEN GLOWING, SPF 30
- Product NDC
- 81522-220
- 11-digit product format
- 815220220
- Labeler code
- 81522
- Product ID
- 81522-220_473bcb90-ab80-170b-e063-6294a90a99d5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sunscreen glowing lotion
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- FSA Store Inc
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 1.5; 4.5; 2.5; 3.5 g/50mL; g/50mL; g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SUNSCREEN GLOWING, SPF 30
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 1.5 g/50mL |
| HOMOSALATE | 4.5 g/50mL |
| OCTISALATE | 2.5 g/50mL |
| OCTOCRYLENE | 3.5 g/50mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81522-220-01 | SUNSCREEN GLOWING, SPF 30 | 50 mL in 1 BOTTLE | LOTION | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 81522-220-01 | 81522022001 | 50 mL in 1 BOTTLE (81522-220-01) | 50 ml | 2025-12-30 | No | No | Historical |