Home DailyMed 2e47343c-a64a-4c75-a7ec-f7eedf7518ea Pain Relieving Foot Spray (IS0235-V1) Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer The Magni Company | Inspec Solutions
Effective date 2026-05-26
Label type HUMAN OTC DRUG LABEL
Version 2
Source full-release
Hydrated at 2026-06-01 02:38:42 Label at a glance# Product DB Foot Pain Relieving
Active ingredient PSEUDOGNAPHALIUM LUTEOALBUM LEAF, GELSEMIUM SEMPERVIRENS WHOLE, APIS MELLIFERA
Label structure 2 sections
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43689-0070-3 DB Foot Pain Relieving 85 g in 1 BOTTLE, SPRAY SPRAY 85 2
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 21 matching rows.
DB Foot Pain Relieving Apis Mellifica, Gelsemium Sempervirens, Gnaphalium WATER CANOLA OIL ETHYLHEXYL STEARATE METHYL SALICYLATE ETHYLHEXYLGLYCERIN CITRIC ACID GLYCERIN SODIUM HYDROXIDE BERGAMOT OIL EUCALYPTUS OIL PHENOXYETHANOL XANTHAN GUM ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) MENTHOL CAMPHOR OIL .ALPHA.-TOCOPHEROL ACETATE, DL- PSEUDOGNAPHALIUM LUTEOALBUM LEAF GELSEMIUM SEMPERVIRENS WHOLE APIS MELLIFERA Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 19 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.