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.
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| Cream | ZINC OXIDE | MONAT GLOBAL CORP | e922d89c-4232-77d8-e053-2995a90a85e5 | 2025-12-26 | Warnings | M020 SOI2LOH54Z |
| Cream | ZINC OXIDE | MONAT GLOBAL CORP | e9231470-9292-0e70-e053-2a95a90a767a | 2025-12-26 | Warnings | M020 SOI2LOH54Z |
| Cream | ZINC OXIDE | MONAT GLOBAL CORP | e92288bb-739a-2f73-e053-2995a90ac01f | 2025-12-26 | Warnings | M020 SOI2LOH54Z |
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| OUHOE Water-Permeable Sunscreen | TITANIUM DIOXIDE | Shantou Ouhoe Technology Co., Ltd. | 46e63e1e-7851-ca26-e063-6394a90a9b53 | 2025-12-26 | Warnings | M020 |
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| Normal Salt | SODIUM CHLORIDE | GRAXCELL PHARMACEUTICAL, LLC | f3f09817-8a38-4aa1-956b-69d9cf695074 | 2025-12-25 | Warnings | 451W47IQ8X |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.