NDC 59062-3301-01 - Babyganics Soothing Itch
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
- 59062-3301
- Requested NDC
- 59062-3301-01
- Package NDCs from labels
- 59062-3301-1, 59062-3301-01
- Manufacturer
- KAS Direct, LLC | Cosmetic Solutions
- Effective date
- 2024-08-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Babyganics Soothing Itch - KAS Direct, LLC | Cosmetic Solutions | KAS Direct, LLC | Cosmetic Solutions | 2024-08-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59062-3301-1 | Babyganics Soothing Itch | 1 in 1 CARTON | STICK | 1 | 1 | |
| 59062-3301-1 | Babyganics Soothing Itch | 18 g in 1 APPLICATOR | STICK | 18 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59062-3301 | BABYGANICS SOOTHING ITCH (OATMEAL) STICK [KAS DIRECT, LLC] | 1 | Current NDC, 2 package rows | 20240901_5c2806fb-5af4-4532-b31a-be77bb23b277.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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.