Sunscreen
- Product NDC
- 41520-769
- 11-digit product format
- 415200769
- Labeler code
- 41520
- Product ID
- 41520-769_4a2bed31-4ba3-4427-e063-6294a90ad1cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- American Sales Company
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-01-12
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 50; 100 mg/mL; 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
- Sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/mL |
| HOMOSALATE | 100 mg/mL |
| OCTISALATE | 50 mg/mL |
| OCTOCRYLENE | 100 mg/mL |
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 |
|---|
| 41520-769-34 | Sunscreen | 236 mL in 1 BOTTLE, PLASTIC | LOTION | 236 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41520-769 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [AMERICAN SALES COMPANY] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250227_79dff6ec-d958-4bba-999b-da4aa67519f5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41520-769-34 | 41520076934 | 236 mL in 1 BOTTLE, PLASTIC (41520-769-34) | 236 ml | 2016-01-12 | 0000-00-00 | No | No | Current |