NDC 59062-1200-01 - suncare essentials
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
- 59062-1200
- Requested NDC
- 59062-1200-01
- Package NDCs from labels
- 59062-1200-1, 59062-1200-2, 59062-1200-01
- Manufacturer
- KAS Direct LLC dba BabyGanics
- Effective date
- 2024-12-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| suncare essentials - KAS Direct LLC dba BabyGanics | KAS Direct LLC dba BabyGanics | 2024-12-26 | HUMAN OTC DRUG LABEL |
| TITANIUM DIOXIDE and ZINC OXIDE - KAS Direct LLC dba BabyGanics | KAS Direct LLC dba BabyGanics | 2024-12-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59062-1200-1 | SPF 50 plus Sunscreen All Mineral Active Ingredients | 13 g in 1 APPLICATOR | STICK | 13 | 3 | |
| 59062-1200-1 | SPF 50 plus Sunscreen All Mineral Active Ingredients | 1 in 1 BLISTER PACK | STICK | 1 | 3 | |
| 59062-1200-2 | SPF 50 plus Sunscreen All Mineral Active Ingredients | 2 in 1 BLISTER PACK | STICK | 2 | 3 | |
| 59062-1200-2 | SPF 50 plus Sunscreen All Mineral Active Ingredients | 13 g in 1 APPLICATOR | STICK | 13 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59062-1200 | SPF 50 PLUS SUNSCREEN ALL MINERAL ACTIVE INGREDIENTS (TITANIUM DIOXIDE AND ZINC OXIDE) STICK KIDS SPF 50 PLUS SUNSCREEN ALL MINERAL ACTIVE INGREDIENTS (TITANIUM DIOXIDE AND ZINC OXIDE) STICK [KAS DIRECT LLC DBA BABYGANICS] | 3 | Current NDC, Legacy NDC, 4 package rows | 20241222_247aae3d-1845-4dd8-b774-b9e8214809a2.zip |
| 59062-1200 | SUNCARE ESSENTIALS (TITANIUM DIOXIDE, OCTISALATE, AND ZINC OXIDE) KIT [KAS DIRECT LLC DBA BABYGANICS] | 2 | Current NDC, Legacy NDC | 20250104_96fd2cf8-cb07-4ec1-8946-8e862f6d8377.zip |
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.