WARTCALM- antimony trisulfide, nitric acid, thuja occidentalis leafy twig, tablet

WartCalm by

Drug Labeling and Warnings

WartCalm by is a Homeopathic medication manufactured, distributed, or labeled by Boiron, Boiron Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients ** (in each tablet)

Antimonium crudum 9C HPUS (0.83 mg) (contains less than 10 -18 mg antimony)

Nitricum acidum 9C HPUS (0.83 mg)

Thuja occidentalis 9C HPUS (0.83 mg)

The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

PURPOSE

Purpose*

Antimonium crudum 9C HPUS (0.83 mg) ... For removal of warts with hard, rough surfaces that often appear in groups

Nitricum acidum 9C HPUS (0.83 mg) ... For removal of yellowish warts that sting

Thuja occidentalis 9C HPUS ... For removal of common warts and plantar warts

INDICATIONS & USAGE

Uses*

• for the removal of common warts. The common wart is easily recognized by the rough "cauliflower-like" appearance on the surface.
• for the 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.

WARNINGS

Warnings

DO NOT USE

Do not use for moles, birthmarks, warts with hair growing on them, genital warts, or warts on the face or mucous membranes.

STOP USE

Stop use and ask a doctor if discomfort persists or if warts become painful, start multiplying quickly, or change in appearance.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

Adults and children 6 years of age and older - Dissolve 2 tablets in the mouth 2 times a day, mornings and evenings, until wart is removed or as directed by a doctor. Daily use for at least 1 month is recommended.

Children 2 to 5 years of age - Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above.

Children under 2 years of age - Ask a doctor.

SPL UNCLASSIFIED SECTION

Other information

• do not use if glued carton and flaps are open or if the blister seal is broken
• store below 86° F (30° C)

INACTIVE INGREDIENT

croscarmellose sodium, lactose, magnesium stearate

QUESTIONS

BoironUSA.com

Info@Boiron.com

1-800-BOIRON-1

(1-800-264-7661)

Made in France

Distributed by Boiron Inc.

Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

Wart Remover*

Common Wart Varieties Planter (Foot) Warts*

Non-scarring Wart Remover*

From the Inside Out

60 meltaway tablets unflavored

Meltaway Tablets Require No Food or Water

No Artificial Colors, Flavors, Sweeteners, or Preservatives

No Known Drug Interactions

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WARTCALM 
antimony trisulfide, nitric acid, thuja occidentalis leafy twig, tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0220-9372
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	9 [hp_C]
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	9 [hp_C]
NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4)	NITRIC ACID	9 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	Boiron
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0220-9372-04	1 in 1 BOX	10/15/2021
1		60 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		10/15/2021

Labeler - Boiron (282560473)

Registrant - Boiron Inc. (014892269)

Establishment
Name	Address	ID/FEI	Business Operations
Boiron		282560473	manufacture(0220-9372)