NDC 67172-020 - Chloraseptic Warming Green Tea
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
- 67172-020
- Package NDCs from labels
- 67172-020-02
- Manufacturer
- Prestige Brands Holdings, Inc.
- Effective date
- 2026-03-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CORN SYRUP - Prestige Brands Holdings, Inc. | Prestige Brands Holdings, Inc. | 2026-03-06 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67172-020-02 | Chloraseptic Warming Green Tea | 18 in 1 BOTTLE | LOZENGE | 18 | 2 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.