Wart Control

Manufacturer
Forces of Nature
Effective date
2026-04-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:38:24

Label at a glance#

ProductWart Control Extra Strength
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, PHYTOLACCA AMERICANA ROOT, THUJA OCCIDENTALIS LEAFY TWIG
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

Active ingredientsPurpose
Thuja Occidentalis* 8XRemedy for Warts
Phytolacca American* 8XHeals Wart Symptoms
Calendula Officinalis* 8XPromotes Healthy Skin and Healing

*Certified Organic

Also Contains

INACTIVE INGREDIENT SECTION

Clove Oil*, Lemon Oil*, Tea Tree Oil*, Thuja Oil*, Thyme Oil*

*Certified Organic

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

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 SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If accidental ingestion and adverse reaction occurs, get medical help or contact a Poison Control Center.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breast-feeding, ask a health professional before use.

OTC - QUESTIONS SECTION

Manufactured by: Forces of Nature, Inc.
21787 8th St East, Sonoma, CA 95476

Questions: 1-877-975-3797

forcesofnaturemedicine.com

RECENT MAJOR CHANGES SECTION

Dosage and Administration - Directions updated for user clarity regarding need to shake before use and continued regimen of application.

PRINCIPAL DISPLAY PANEL - 4 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HOMEOPATHIC

NDC #51393-7434-1

FORCES OF NATURE ®

TRUSTED PLANT REMEDIES

Wart

Control®

EXTRA STRENGTH

REMOVES COMMON & PLANTAR WARTS

with Northern White Cedar & Marigold

  • Targets warts at the root
  • For hands, feet, & fingers
  • No acids, burning, or freezing

NON

GMO

Project

VERIFIED

nongmoproject.org

USDA

ORGANIC

11ml (0.37 FL OZ)

Wart Control 11mlWart Control 11ml

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130830743009127GTIN-13: 0830743009127
EAN-13: 0830743009127
GTIN-12: 830743009127
UPC-A: 830743009127
GTIN storage (14 digits): 00830743009127
Wart Control 11ml Carton.jpg

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-7434-1Wart ControlExtra Strength11 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS114
51393-7434-2Wart ControlExtra Strength33 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS334
51393-7434-4Wart ControlExtra Strength4 mL in 1 BOTTLESOLUTION/ DROPS44

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CALENDULA OFFICINALIS FLOWERING TOPACTIVE INGREDIENT18E7415PXQ1
PHYTOLACCA AMERICANA ROOTACTIVE INGREDIENT11E6VI8VEG1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
CALENDULA OFFICINALIS FLOWERING TOPACTIVE MOIETY18E7415PXQ1
PHYTOLACCA AMERICANA ROOTACTIVE MOIETY11E6VI8VEG1
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
CEDAR LEAF OILINACTIVE INGREDIENTBJ169U4NLG1
Clove OilINACTIVE INGREDIENT578389D6D01
Lemon OilINACTIVE INGREDIENTI9GRO824LL1
Palmarosa OilINACTIVE INGREDIENT0J3G3O53ST1
Tea Tree OilINACTIVE INGREDIENTVIF565UC2G1
Thyme OilINACTIVE INGREDIENT2UK410MY6B1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51393-743451393-7434-1, 51393-7434-2, 51393-7434-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 16 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Clove OilCLOVE OIL578389D6D0PASTE, DENTIFRICE / DENTAL2.4 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0SUSPENSION / ORAL0.1 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Lemon OilLEMON OIL, COLD PRESSEDI9GRO824LLGEL / TOPICAL0.05 %w/wExact identifier — unii+route
4 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0SUSPENSION / ORAL0.1 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0PASTE, DENTIFRICE / DENTAL2.4 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Lemon OilLEMON OIL, COLD PRESSEDI9GRO824LLGEL / TOPICAL0.05 %w/wExact identifier — unii+route
4 equally ranked IID candidates
Lemon OilLEMON OIL, COLD PRESSEDI9GRO824LLGEL / TOPICAL0.05 %w/wExact identifier — unii+route
4 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0PASTE, DENTIFRICE / DENTAL2.4 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0SUSPENSION / ORAL0.1 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0ELIXIR / ORAL0.42 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0SUSPENSION / ORAL0.1 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0ELIXIR / ORAL0.42 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0ELIXIR / ORAL0.42 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates
Lemon OilLEMON OIL, COLD PRESSEDI9GRO824LLGEL / TOPICAL0.05 %w/wExact identifier — unii+route
4 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0PASTE, DENTIFRICE / DENTAL2.4 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
Clove OilCLOVE OIL578389D6D0ELIXIR / ORAL0.42 mg/5mlExact identifier — unii candidate
12 equally ranked IID candidates

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
Wart Control Extra StrengthCALENDULA OFFICINALIS FLOWERING TOP, PHYTOLACCA AMERICANA ROOT, AND THUJA OCCIDENTALIS LEAFY TWIGForces of Nature7c6b837e-aff9-4a77-99d6-a4d0f5dbd9f82026-04-24WarningsExact identifier
ndc (package): 51393-7434-2
ndc (package): 51393-7434-1
ndc (package): 51393-7434-4
ndc (product): 51393-7434
ndc11 (package): 51393743402
ndc11 (package): 51393743404
ndc11 (package): 51393743401
spl id: 5036d4fd-e8ca-1877-e063-6294a90a444b
spl set id: 7c6b837e-aff9-4a77-99d6-a4d0f5dbd9f8

Reported adverse events (FAERS/openFDA)#

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