NDC 79265-8065-01 - Babo Baby Face Mineral Sunscreen
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
- 79265-8065
- Requested NDC
- 79265-8065-01
- Package NDCs from labels
- 79265-8065-1, 79265-8065-01
- Manufacturer
- Babo Botanicals, Inc.
- Effective date
- 2024-12-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 8065 Babo Baby Face SPF 50 Mineral Sunscreen Stick | Babo Botanicals, Inc. | 2024-12-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79265-8065-1 | Babo Baby Face Mineral Sunscreen | 1 in 1 CARTON | STICK | 1 | 7 | |
| 79265-8065-1 | Babo Baby Face Mineral Sunscreen | 17 g in 1 TUBE | STICK | 17 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79265-8065 | BABO BABY FACE MINERAL SUNSCREEN (MINERAL SUNSCREEN) STICK [BABO BOTANICALS, INC.] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241215_b131664d-1ad2-0a2f-e053-2995a90acbda.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.