Sunnyscreen SPF 50
- Product NDC
- 75936-252
- Requested package NDC
- 75936-252-01
- 11-digit product format
- 759360252
- Labeler code
- 75936
- Product ID
- 75936-252_ec0be7c6-8f41-9c89-e053-2995a90ab120
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Supergoop, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-04-02
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 10 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75936-252-01 | Sunnyscreen SPF 50 | 100 mL in 1 BOTTLE, SPRAY | SPRAY | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75936-252 | SUNNYSCREEN SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) SPRAY [SUPERGOOP, LLC] | 4 | Legacy NDC, 1 package rows | 20241220_859461ea-582e-8185-e053-2991aa0a954a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75936-252-01 | 75936025201 | 100 mL in 1 BOTTLE, SPRAY (75936-252-01) | 100 ml | 2019-04-02 | 0000-00-00 | No | No | Current |