FDA label 400a6f70-4381-5edb-e063-6294a90a0224
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
- SPL set ID
- 62f15711-1f75-446d-bdd4-881b40e3eeab
- SPL ID
- 400a6f70-4381-5edb-e063-6294a90a0224
- Version
- 18
- Effective date
- 2025-09-30
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:31:41
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 |
|---|---|---|---|
| spl id | 400a6f70-4381-5edb-e063-6294a90a0224 | id | |
| spl set id | 62f15711-1f75-446d-bdd4-881b40e3eeab | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings For external use only When using this product avoid contact with the eyes Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTION *This product is not manufactured or distributed by Dickinson Brands, Inc., distributor of T.N. Dickinson's ® Witch Hazel. Distributed by Target Corporation Minneapolis, MN 55403 Made in U.S.A. with US and foreign components ©2015 Target Brands, Inc. Shop Target.com Questions? Call 1-800-910-6874 Pat. D675, 101
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.