NDC 73676-217-01 - Abib Heartleaf mild sunscreen Relief tube
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
- 73676-217
- Requested NDC
- 73676-217-01
- Package NDCs from labels
- 73676-217-01, 73676-217-02
- Manufacturer
- FOURCOMPANY CO., LTD. | Cosmax, Inc.
- Effective date
- 2025-05-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Abib Heartleaf mild sunscreen Relief tube - FOURCOMPANY CO., LTD. | Cosmax, Inc. | FOURCOMPANY CO., LTD. | Cosmax, Inc. | 2025-05-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73676-217-01 | Abib Heartleaf mild sunscreen Relief tube | 50 mL in 1 TUBE | CREAM | 50 | 1 | |
| 73676-217-02 | Abib Heartleaf mild sunscreen Relief tube | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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.