Pain Relieving Foot Spray (IS0235-V1)

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#

ProductDB Foot Pain Relieving
Active ingredientPSEUDOGNAPHALIUM LUTEOALBUM LEAF, GELSEMIUM SEMPERVIRENS WHOLE, APIS MELLIFERA
Label structure2 sections

Label contents#

Full prescribing information#

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water
Alkyl Glucoside
Canola Oil
Ethylhexyl Stearate
Methyl Salicylate
Ethylhexylglycerin
Citric Acid (Kosher)
Calmiskin GR
Glycerin
Sodium Hydroxide
Citrus Aurantium Bergamia (Bergamot) Fruit Oil
Eucalyptus Globulus Leaf Oil
Phenoxyethanol
Xanthan Gum
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Menthol
Camphor Flakes
Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0070-3DB Foot Pain Relieving85 g in 1 BOTTLE, SPRAYSPRAY852

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43689-007043689-0070-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DB Foot Pain RelievingAPIS MELLIFICA, GELSEMIUM SEMPERVIRENS, GNAPHALIUMThe Magni Company2e47343c-a64a-4c75-a7ec-f7eedf7518ea2026-05-26WarningsExact identifier
ndc (package): 43689-0070-3
ndc (product): 43689-0070
ndc11 (package): 43689007003
spl id: 52b905b2-0678-bf51-e063-6294a90a3d11
spl set id: 2e47343c-a64a-4c75-a7ec-f7eedf7518ea

Reported adverse events (FAERS/openFDA)#

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