Sunnyscreen SPF 50
- Product NDC
- 75936-250
- Requested package NDC
- 75936-250-01
- 11-digit product format
- 759360250
- Labeler code
- 75936
- Product ID
- 75936-250_ec577d44-9079-ec2a-e053-2a95a90aa26f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Supergoop, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-04-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 3 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.
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75936-250-01 | Sunnyscreen SPF 50 | 89 mL in 1 BOTTLE | LOTION | 89 | | 6 |
| 75936-250-02 | Sunnyscreen SPF 50 | 5 mL in 1 PACKET | LOTION | 5 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75936-250 | SUNNYSCREEN SPF 50 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [SUPERGOOP, LLC] | 6 | Legacy NDC, 2 package rows | 20231215_857ef2e1-31da-7647-e053-2991aa0a94f5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75936-250-01 | 75936025001 | 89 mL in 1 BOTTLE (75936-250-01) | 89 ml | 2019-04-01 | 0000-00-00 | No | No | Current |