FDA.reportPublic FDA data

Foot Pain Relieving

Manufacturer
The Magni Group Inc | United Laboratories Manufacturing LLC
Effective date
2020-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:03

Label at a glance#

ProductFoot Pain Relieving
Active ingredientAPIS MELLIFERA, GELSEMIUM SEMPERVIRENS ROOT, PSEUDOGNAPHALIUM LUTEOALBUM LEAF
Label structure12 sections

Dosage and administration

NDC: 43689-0040

Label contents#

Full prescribing information#

Active Ingredients (In Spray) - Purpose Apis Mellifica 3X HPUS - Relieves Foot Pain Gnaphalium 3X HPUS - Relieves Foot Pain Gelsemium Sempervirens 6X HPUS - External Analgesic

OTC - ACTIVE INGREDIENT SECTION

Pain Relieving Foot SprayPain Relieving Foot Spray

NDC: 43689-0040

Purpose: Relieves Foot Pain External Analgesic

OTC - PURPOSE SECTION

NDC: 43689-0040

Use: Temporarily relieves foot pain

INDICATIONS & USAGE SECTION

NDC: 43689-0040

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

NDC:

Warning: For external use only

WARNINGS SECTION

NDC: 43689-0040

When using this product: - Avoid contact with eyes

OTC - WHEN USING SECTION

NDC: 43689-0040

If symptoms persist for more than 7 days or worsen, consult your physician

OTC - ASK DOCTOR SECTION

NDC: 43689-0040

Do not use on open wounds, cuts, damaged, or infected skin

OTC - DO NOT USE SECTION

NDC: 43689-0040

Directions: - Adults and children 12 years of age and older, apply to all surfaces of the feet, heels and toes up to four times daily - Apply to legs as needed

DOSAGE & ADMINISTRATION SECTION

NDC: 43689-0040

Other information: - Most beneficial when applied after bathing, showering, or a foot soak - The letter "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States - These statements ar...

OTHER SAFETY INFORMATION

NDC: 43689-0040

Inactive Ingredients: Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzoic Acid, Bergamot Oil, C14-22 Alcohol/C12-20 Alkyl Glucoside, Canola Oil, Camphor Gum, Citric Acid, Ethylhexyl Stearate, Eucalyptus Oil, Glycerin, Mentha Piperita (Peppermint) Extract,...

INACTIVE INGREDIENT SECTION

NDC: 43689-0040

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

NDC: 43689-0040

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43689-0040-12023-01-30C16284748780-1f386c64a-2daa-0266-e053-dadaa90a7c1ab072c546-7806-52cb-e053-2a95a90ab1b4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0040-1Foot Pain Relieving85 g in 1 BOTTLE, SPRAYSPRAY851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43689-0040FOOT PAIN RELIEVING (APIS MELLIFICA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM) SPRAY [THE MAGNI GROUP INC]1Legacy NDC, 1 package rows20201230_b072c546-7806-52cb-e053-2a95a90ab1b4.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43689-004043689-0040-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SORBIC ACIDX045WJ989BIACT
GLYCERINPDC6A3C0OXIACT
APIS MELLIFERA7S82P3R43ZACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
C14-22 ALCOHOLSB1K89384RJIACT
CANOLA OIL331KBJ17RKIACT
METHYL SALICYLATELAV5U5022YIACT
MENTHA X PIPERITA WHOLE79M2M2UDA9IACT
BERGAMOT OIL39W1PKE3JIIACT
XANTHAN GUMTTV12P4NEEIACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
PSEUDOGNAPHALIUM LUTEOALBUM LEAFBGI20Z6M57ACTIB
C12-20 ALKYL GLUCOSIDEK67N5Z1RUAIACT
BENZOIC ACID8SKN0B0MIMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
SODIUM HYDROXIDE55X04QC32IIACT
PANTHENOLWV9CM0O67ZIACT
EUCALYPTUS OIL2R04ONI662IACT
MENTHOLL7T10EIP3AIACT
WATER059QF0KO0RIACT

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
b072c546-7807-52cb-e053-2a95a90ab1b4b072c546-7806-52cb-e053-2a95a90ab1b42020-12-29WarningsExact identifier
spl id: b072c546-7807-52cb-e053-2a95a90ab1b4
spl set id: b072c546-7806-52cb-e053-2a95a90ab1b4

Reported adverse events (FAERS/openFDA)#

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