NDC 75936-129-01 - Skin Soothing Mineral Sunscreen Broad Spectrum SPF 40 Supergoop
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 75936-129
- Requested NDC
- 75936-129-01
- Package NDCs from labels
- 75936-129-01, 75936-129-02, 75936-129-03, 75936-129-04
- Manufacturer
- TAYLOR JAMES, LTD. | Cosway Company Inc
- Effective date
- 2018-12-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Octinoxate, Zinc Oxide - TAYLOR JAMES, LTD. | Cosway Company Inc | TAYLOR JAMES, LTD. | Cosway Company Inc | 2018-12-18 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75936-129-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-23fe-a910-e053-dadaa90a0b85 | Skin Soothing Mineral Sunscreen SPF 40 |
| 75936-129-04 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-23fe-a910-e053-dadaa90a0b85 | Skin Soothing Mineral Sunscreen SPF 40 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75936-129-01 | Skin Soothing Mineral Sunscreen Broad Spectrum SPF 40Supergoop | 71 mL in 1 BOTTLE | CREAM | 71 | 6 | |
| 75936-129-02 | Skin Soothing Mineral Sunscreen Broad Spectrum SPF 40Supergoop | 1 in 1 BOX | CREAM | 1 | 6 | |
| 75936-129-03 | Skin Soothing Mineral Sunscreen Broad Spectrum SPF 40Supergoop | 30 mL in 1 BOTTLE | CREAM | 30 | 6 | |
| 75936-129-04 | Skin Soothing Mineral Sunscreen Broad Spectrum SPF 40Supergoop | 1 in 1 BOX | CREAM | 1 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.