Walgreens Cold Therapy Pain Relief Foot Cream

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: Walgreens Cold Therapy Pain Relief Foot Cream
Generic name: MENTHOL
Manufacturer: Walgreen Co.
Product type: HUMAN OTC DRUG
SPL set ID: 3bc8ece3-d555-3efb-e063-6394a90a1981
SPL ID: 4d29da93-9321-934c-e063-6394a90a74af
Version: 2
Effective date: 2026-03-16
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:12:33

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		M017	openfda.application_number
brand name		Walgreens Cold Therapy Pain Relief Foot Cream	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Walgreen Co.	openfda.manufacturer_name
ndc	package	0363-1292-04	openfda.package_ndc
ndc	product	0363-1292	openfda.product_ndc
ndc11	package	00363129204	derived:openfda.package_ndc
rxcui		253020	openfda.rxcui
spl id		4d29da93-9321-934c-e063-6394a90a74af	id
spl set id		3bc8ece3-d555-3efb-e063-6394a90a1981	set_id
unii		L7T10EIP3A	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 Avoid contact with the eyes or mucous membranes Do not apply to wounds or damaged skin Do not use with other ointments, creams, sprays or liniments Do not apply to irritated skin or if excessive irritation develops Do not bandage Wash hands after use with cool water Do not use with heating pad or device Stop use and ask a doctor if Condition worsens, or if symptoms persist for more than 7 days, or clear up and recur If pregnant or breastfeeding Ask a health professional before use. Keep out of reach of children. If accidientally ingested, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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