NDC 83403-101-01 - BETA-GLUCAN MILD 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
- 83403-101
- Requested NDC
- 83403-101-01
- Package NDCs from labels
- 83403-101-01, 83403-101-02
- Manufacturer
- IUNIK Co., Ltd | UCL Co., Ltd.
- Effective date
- 2026-01-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BETA-GLUCAN MILD SUNSCREEN | IUNIK Co., Ltd | UCL Co., Ltd. | 2026-01-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83403-101-01 | BETA-GLUCAN MILD SUNSCREEN | 60 mL in 1 TUBE | LOTION | 60 | 1 | |
| 83403-101-02 | BETA-GLUCAN MILD SUNSCREEN | 1 in 1 BOX | LOTION | 1 | 1 |
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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| Biotrue Hydration Boost | GLYCERIN | Bausch & Lomb Incorporated | e2621477-e6ee-4275-ba0a-939dca2550c4 | 2025-05-19 | Warnings | PDC6A3C0OX |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.