Sunscreen SPF 30
- Product NDC
- 49757-012
- 11-digit product format
- 497570012
- Labeler code
- 49757
- Product ID
- 49757-012_485b2ce6-669f-afc0-e063-6394a90ad9b7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone 3% , Homosalate 10%,Octisalate 5%
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Rocky Mountain
- Application
- M20
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-21
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE
- Active strength
- 3; 10; 5 g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunscreen SPF 30
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 3 g/100g |
| HOMOSALATE | 10 g/100g |
| OCTISALATE | 5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49757-012-06 | Sunscreen SPF 30 | 170 g in 1 CONTAINER | SPRAY | 170 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 49757-012-06 | 49757001206 | 170 g in 1 CONTAINER (49757-012-06) | 170 g | 2025-08-21 | No | No | Current |