NDC 73656-037 - Optimax Professional Whitening Anticavity Fluoride
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
- 73656-037
- Package NDCs from labels
- 73656-037-00
- Manufacturer
- WHITE GLO USA INC
- Effective date
- 2025-09-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Optimax Professional Whitening Anticavity Fluoride - WHITE GLO USA INC | WHITE GLO USA INC | 2025-09-18 | HUMAN OTC DRUG LABEL |
| Optimax Professional Whitening Anticavity Fluoride - WHITE GLO USA INC | WHITE GLO USA INC | 2025-09-18 | HUMAN OTC DRUG LABEL |
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.