Db Foot Pain Relieving
FDA Label NDC 43689-0039

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Magni Group Inc for the product Db Foot Pain Relieving (NDC 43689-0039). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients (in spray) - purpose apis mellifica 3x hpus - relieves foot pain gnaphalium 3x hpus - relieves foot pain gelsemium sempervirens 6x hpus - external analgesic, purpose: relieves foot pain external analgesic, use: temporarily relieves foot pain, keep out of reach of children, warnings: for external use only, when using this product: - avoid contact with eyes, if symptoms persist for more than 7 days or worsen, consult your physician, do not use on open wounds, cuts, damaged, or infected skin, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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