SPF 50 SUNSCREEN
- Product NDC
- 53942-001
- 11-digit product format
- 539420001
- Labeler code
- 53942
- Product ID
- 53942-001_24afa50a-41c5-f549-e063-6394a90a23f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- DEMOULAS SUPER MARKETS, INC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-01-28
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 50; 40 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SPF 50 SUNSCREEN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/g |
| HOMOSALATE | 100 mg/g |
| OCTISALATE | 50 mg/g |
| OCTOCRYLENE | 40 mg/g |
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 |
|---|
| 53942-001-37 | SPF 50 SUNSCREEN | 156 g in 1 CAN | AEROSOL, SPRAY | 156 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53942-001 | SPF 50 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) AEROSOL, SPRAY [DEMOULAS SUPER MARKETS, INC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241019_ee782436-9eff-49e4-8edc-fd9783454c07.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53942-001-37 | 53942000137 | 156 g in 1 CAN (53942-001-37) | 156 g | 2015-01-28 | 0000-00-00 | No | No | Current |