Wart Control Extra Strength
Wart Control Extra Strength is an FDA drug label for the active ingredient CALENDULA OFFICINALIS FLOWERING TOP, PHYTOLACCA AMERICANA ROOT, AND THUJA OCCIDENTALIS LEAFY TWIG manufactured by Forces of Nature administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260424.
- Generic name
- CALENDULA OFFICINALIS FLOWERING TOP, PHYTOLACCA AMERICANA ROOT, AND THUJA OCCIDENTALIS LEAFY TWIG
- Manufacturer
- Forces of Nature
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 51393-7434
- Application
- N/A
- Label effective
- 20260424
About this product
Wart Control Extra Strength is an FDA-registered drug product whose active ingredient is CALENDULA OFFICINALIS FLOWERING TOP, PHYTOLACCA AMERICANA ROOT, AND THUJA OCCIDENTALIS LEAFY TWIG. It is labelled by Forces of Nature taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 51393-7434, label effective 20260424. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing CALENDULA OFFICINALIS FLOWERING TOP, PHYTOLACCA AMERICANA ROOT, AND THUJA OCCIDENTALIS LEAFY TWIG are most often described in connection with: removal common, wart easily, rough cauliflower-like, plantar warts, location only, footprint pattern. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Indications For the treatment and removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. For the treatment and removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern.
Dosage & Administration
Directions Shake well before use. Apply directly or put a few drops on a moistened cotton swab and dab on wart(s) 3 times per day. Continue until the wart is no longer visible. Putting a band-aid over the wart after application may be of benefit and expedite the healing process.
Warnings
Warnings For external use only. Some individuals may be sensitive to essential oils. Begin with a small drop to determine if the product causes any increased redness or irritation. Discontinue use if any irritation occurs.Stop use and consult a doctor if condition worsens. Not for use on children under the age of 2 without physician direction. Keep out of the reach of children. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center. If you are pregnant or breast-feeding, ask a health professional before use.
Frequently asked questions
What is Wart Control Extra Strength used for?
Indications For the treatment and removal of common warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. For the treatment and removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern.
Who makes Wart Control Extra Strength?
Forces of Nature is the labeler of record for Wart Control Extra Strength.
What form does Wart Control Extra Strength come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Wart Control Extra Strength prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Wart Control Extra Strength been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.