medicated 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 (canonical bytes are SHA-256 checked before publication)

Brand name: medicated pads
Generic name: WITCH HAZEL
Manufacturer: TARGET CORPORATION
Product type: HUMAN OTC DRUG
SPL set ID: acd0d99d-2a77-4227-bebb-c819f4a52666
SPL ID: 412203ce-d7fc-28ee-e063-6394a90a929f
Version: 6
Effective date: 2025-10-14
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:52:48

Harmonized routes table
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.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		medicated pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		TARGET CORPORATION	openfda.manufacturer_name
ndc	package	11673-614-10	openfda.package_ndc
ndc	product	11673-614	openfda.product_ndc
ndc11	package	11673061410	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
spl id		412203ce-d7fc-28ee-e063-6394a90a929f	id
spl set id		acd0d99d-2a77-4227-bebb-c819f4a52666	set_id
unii		101I4J0U34	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. When using this product do not exceed the recommended daily dosage unless directed by a doctor. do not insert into rectum or vagina using fingers or mechanical device. Stop use and ask a doctor if rectal bleeding occurs condition worsens or does not improve within 7 days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.