Zinc Screen Broad Spectrum Sunscreen SPF 40
- Product NDC
- 75936-223
- 11-digit product format
- 759360223
- Labeler code
- 75936
- Product ID
- 75936-223_ebca053c-c526-79b2-e053-2a95a90a8cf5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Supergoop, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-04-30
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 13 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75936-223-01 | Zinc Screen Broad Spectrum Sunscreen SPF 40 | 50 mL in 1 BOTTLE | LOTION | 50 | | 6 |
| 75936-223-02 | Zinc Screen Broad Spectrum Sunscreen SPF 40 | 10 mL in 1 BOTTLE | LOTION | 10 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75936-223 | ZINC SCREEN BROAD SPECTRUM SUNSCREEN SPF 40 (ZINC OXIDE) LOTION [SUPERGOOP, LLC] | 6 | Legacy NDC, 2 package rows | 20241208_87adf142-7560-30d9-e053-2a95a90aca90.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75936-223-01 | 75936022301 | 50 mL in 1 BOTTLE (75936-223-01) | 50 ml | 2019-04-30 | 0000-00-00 | No | No | Current |
| 75936-223-02 | 75936022302 | 10 mL in 1 BOTTLE (75936-223-02) | 10 ml | 2020-11-19 | 0000-00-00 | No | No | Current |