Walgreens Pain Relieving Foot Pain Relief

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 Pain Relieving Foot Pain Relief
Generic name
APIS MELLIFERA, GELSEMIUM SEMPERVIRENS WHOLE, AND PSEUDOGNAPHALIUM LUTEOALBUM LEAF
Manufacturer
Walgreen Company
Product type
HUMAN OTC DRUG
SPL set ID
6c6cbae1-e2a9-43bf-9bfc-a20e9d22cc58
SPL ID
44eaa7ef-039f-4615-a103-cb923d14e5ce
Version
2
Effective date
2023-02-27
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:46
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use on damaged skin, open wounds, or mucous membranes According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms). Avoid contact with the eyes Do not use if you are allergic to Apis mellifica, Gelsenium sempervirens, Gmaphalium or any of this product's inactive ingredients. Do not bandage tightly Do not use with heating pads or other heating devices. When using this product avoid contact with eyes. If pregnant, trying to get pregnant or breast-feeding , ask a health professional before use. Stop use and ask a doctor if conditions worsen or if symptoms persist for more than 72 hours or clear up and occur again within a few days. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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