warnings
Warnings For external rectal use only Stop use and ask doctor if rectal bleeding or continued irritation occurs
AER Pre-moistened Witch Hazel Pad
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
- AER Pre-moistened Witch Hazel Pad
- Generic name
- WITCH HAZEL
- Manufacturer
- Birchwood Laboratories LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1cca622f-0a6b-4f35-9355-34c249ee705e
- SPL ID
- 2baae3c5-a04e-c51e-e063-6394a90a81c3
- Version
- 6
- Effective date
- 2025-01-14
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:58:27
| Harmonized routes |
|---|
| RECTAL, 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 | AER Pre-moistened Witch Hazel Pad | openfda.brand_name | |
| generic name | WITCH HAZEL | openfda.generic_name | |
| manufacturer name | Birchwood Laboratories LLC | openfda.manufacturer_name | |
| ndc | package | 50289-3250-1 | openfda.package_ndc |
| ndc | product | 50289-3250 | openfda.product_ndc |
| ndc11 | package | 50289325001 | derived:openfda.package_ndc |
| rxcui | 1247719 | openfda.rxcui | |
| rxcui | 844379 | openfda.rxcui | |
| spl id | 2baae3c5-a04e-c51e-e063-6394a90a81c3 | id | |
| spl set id | 1cca622f-0a6b-4f35-9355-34c249ee705e | 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.