Label: WARTCALM- antimony trisulfide, nitric acid, thuja occidentalis leafy twig, tablet
- NDC Code(s): 0220-9372-04
- Packager: Boiron
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated April 13, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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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
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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
- DO NOT USE
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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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
- INACTIVE INGREDIENT
- QUESTIONS
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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
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INGREDIENTS AND APPEARANCE
WARTCALM
antimony trisulfide, nitric acid, thuja occidentalis leafy twig, tabletProduct 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)
