NDC 67732-822 - Witch Hazel
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
- 67732-822
- Package NDCs from labels
- 67732-822-43
- Manufacturer
- Duane Reade | Vi-Jon
- Effective date
- 2020-05-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Witch Hazel - Duane Reade | Vi-Jon | Duane Reade | Vi-Jon | 2020-05-19 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| WITCH HAZEL | ACTIVE INGREDIENT | 101I4J0U34 | WITCH HAZEL LIQUID [DUANE READE] | 1 | |
| WITCH HAZEL | ACTIVE MOIETY | 101I4J0U34 | WITCH HAZEL LIQUID [DUANE READE] | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | WITCH HAZEL LIQUID [DUANE READE] | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.