warnings
Warnings: For external use only When using this product do not exceed recommended dosage unless recommended by a physician do not put this product into rectum by using fingers or any mechanical device or applicator
TN Dickinsons Witch Hazel Hemorrhoidal Pads
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
- TN Dickinsons Witch Hazel Hemorrhoidal Pads
- Generic name
- WITCH HAZEL
- Manufacturer
- Dickinson Brands Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1b50f4dc-c26a-431a-ae18-c43513871b39
- SPL ID
- 6a5d0b28-b31d-43df-a612-ef3b137a0621
- Version
- 6
- Effective date
- 2024-12-18
- Source export date
- 2026-11-06
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:39:56
| 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 | M015 | openfda.application_number | |
| brand name | TN Dickinsons Witch Hazel Hemorrhoidal Pads | openfda.brand_name | |
| generic name | WITCH HAZEL | openfda.generic_name | |
| manufacturer name | Dickinson Brands Inc. | openfda.manufacturer_name | |
| ndc | package | 52651-003-01 | openfda.package_ndc |
| ndc | product | 52651-003 | openfda.product_ndc |
| ndc11 | package | 52651000301 | derived:openfda.package_ndc |
| rxcui | 844379 | openfda.rxcui | |
| spl id | 6a5d0b28-b31d-43df-a612-ef3b137a0621 | id | |
| spl set id | 1b50f4dc-c26a-431a-ae18-c43513871b39 | set_id | |
| unii | 101I4J0U34 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.