Wart Freee
FDA Label NDC 57955-5059

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by King Bio Inc. for the product Wart Freee (NDC 57955-5059). 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 otc - active ingredient, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, other safety information, otc - purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Drug Facts

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HPUS active ingredients: Antimonium crudum, Causticum, Dulcamara, Kali muriaticum, Nitricum acidum, Sabina, Staphysagria, Sulphur, Thuja occidentalis.

Indications & Usage

Uses a natural aid for:

  • smooth or rough warts
  • itching, burning vesicles
  • dry, scaly, unhealthy skin

Warnings

Warnings

  • If symptoms persist or worsen, seek advice of a physician.
  • If pregnant or breast-feeding, ask a healthcare professional before use.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

Directions:

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Adults: 3 sprays 3 times per day.
  • Children 2-12 years: 2 sprays 3 times per day.
  • Use additionally as needed, up to 6 times per day.

Inactive Ingredient

Inactive ingredients: Bio-Energetically Enhanced™ pure water, citric acid, potassium sorbate.

Other Safety Information

Tamper resistant for your protection. Use only if safety seal is intact.

Otc - Purpose

Uses a natural aid for: •smooth or rough warts •itching •burning vesicles dry, scaly, unhealthy skin

* Please review the disclaimer below.