Tucks Medicated Cooling 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: Tucks Medicated Cooling Pads
Generic name: WITCH HAZEL
Manufacturer: Blistex Inc
Product type: HUMAN OTC DRUG
SPL set ID: b3e68008-3d0d-4124-9579-b503e9fb95c9
SPL ID: 7b87eeff-5bf9-4f03-b38a-5d7557ce49bf
Version: 10
Effective date: 2024-12-13
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:33:03

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Tucks Medicated Cooling Pads	openfda.brand_name
generic name		WITCH HAZEL	openfda.generic_name
manufacturer name		Blistex Inc	openfda.manufacturer_name
ndc	package	10157-2103-3	openfda.package_ndc
ndc	package	10157-2103-4	openfda.package_ndc
ndc	package	10157-2103-2	openfda.package_ndc
ndc	package	10157-2103-1	openfda.package_ndc
ndc	product	10157-2103	openfda.product_ndc
ndc11	package	10157210301	derived:openfda.package_ndc
ndc11	package	10157210304	derived:openfda.package_ndc
ndc11	package	10157210302	derived:openfda.package_ndc
ndc11	package	10157210303	derived:openfda.package_ndc
rxcui		844379	openfda.rxcui
rxcui		1247709	openfda.rxcui
spl id		7b87eeff-5bf9-4f03-b38a-5d7557ce49bf	id
spl set id		b3e68008-3d0d-4124-9579-b503e9fb95c9	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 use more than directed unless told to do so by a doctor do not put directly in the rectum by using fingers or any mechanical device or applicator 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.

Reported adverse events (FAERS/openFDA)#

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