warnings
Warnings For external use only
Witch Hazel
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Witch Hazel
- Generic name
- WITCH HAZEL
- Manufacturer
- United Natural Foods, Inc. dba UNFI
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d2d1bd9e-7025-4151-95f2-a2f521dc2be8
- SPL ID
- 5a1d8c66-d618-9cbe-e063-6394a90ab118
- Version
- 20
- Effective date
- 2026-08-28
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:43
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M016 | openfda.application_number | |
| brand name | Witch Hazel | openfda.brand_name | |
| generic name | WITCH HAZEL | openfda.generic_name | |
| manufacturer name | United Natural Foods, Inc. dba UNFI | openfda.manufacturer_name | |
| ndc | package | 41163-822-43 | openfda.package_ndc |
| ndc | product | 41163-822 | openfda.product_ndc |
| ndc11 | package | 41163082243 | derived:openfda.package_ndc |
| rxcui | 200295 | openfda.rxcui | |
| spl id | 5a1d8c66-d618-9cbe-e063-6394a90ab118 | id | |
| spl set id | d2d1bd9e-7025-4151-95f2-a2f521dc2be8 | set_id | |
| unii | 101I4J0U34 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse event Like it or let us make it right. That's our quality promise. 855-423-2630 DISTRIBUTED BY UNFI PROVIDENCE, RI 02903 USA Pat. D675, 101
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.