FDA.reportPublic FDA data

DB 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#

ProductDB Foot Pain Relieving
Active ingredientPSEUDOGNAPHALIUM LUTEOALBUM LEAF, APIS MELLIFERA, GELSEMIUM SEMPERVIRENS ROOT
Label structure12 sections

Dosage and administration

NDC: 43689-0039

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 Spray DBPain Relieving Foot Spray DB

NDC: 43689-0039

Purpose: Relieves Foot Pain External Analgesic

OTC - PURPOSE SECTION

NDC: 43689-0039

Use: Temporarily Relieves Foot Pain

INDICATIONS & USAGE SECTION

NDC: 43689-0039

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

NDC: 43689-0039

Warnings: For external use only

WARNINGS SECTION

NDC: 43689-0039

When using this product: - Avoid contact with eyes

OTC - WHEN USING SECTION

NDC: 43689-0039

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

OTC - ASK DOCTOR SECTION

NDC: 43689-0039

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

OTC - DO NOT USE SECTION

NDC: 43689-0039

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

DOSAGE & ADMINISTRATION SECTION

NDC: 43689-0039

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

OTHER SAFETY INFORMATION

NDC: 43689-0039

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: 43689-0039

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel DBPrincipal Display Panel DB

NDC: 43689-0039

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
43689-0039-12023-01-30C16284748780-1f386c649-a1f1-0266-e053-dadaa90a7c1ab06c4a3e-2c69-3a9c-e053-2a95a90a4fb8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0039-1DB Foot Pain Relieving85 g in 1 BOTTLE, SPRAYSPRAY851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43689-0039DB FOOT PAIN RELIEVING (APIS MELLIFICA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM) SPRAY [THE MAGNI GROUP INC]1Legacy NDC, 1 package rows20201230_b06c4a3e-2c69-3a9c-e053-2a95a90a4fb8.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
43689-003943689-0039-1

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

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
b06c4a3e-2c6a-3a9c-e053-2a95a90a4fb8b06c4a3e-2c69-3a9c-e053-2a95a90a4fb82020-12-29WarningsExact identifier
spl id: b06c4a3e-2c6a-3a9c-e053-2a95a90a4fb8
spl set id: b06c4a3e-2c69-3a9c-e053-2a95a90a4fb8

Reported adverse events (FAERS/openFDA)#

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