Label: ANTI-WART- bufo rana, buxus sempervirens, juglans regia, nitricum acidum, oleander, stannum metallicum, sulphur, taxus baccata, thuja occidentalis, vanadium metallicum liquid

  • Category: HUMAN OTC DRUG LABEL

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 December 18, 2019

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  • ACTIVE INGREDIENT

    Active ingredients
    Each drop contains:
    Bufo rana (European toad) Venom 12X
    Buxus sempervirens (Boxwood) Leaf and Twig 6X
    Juglans regia (English walnut) Leaf and Pericarp 2X
    Nitricum acidum (Nitric acid) 10X
    Oleander (Rose laurel) Leaf 6X
    Stannum metallicum (Tin) 10X
    Sulphur (Sublimed sulfur) 10X
    Taxus baccata (Yew) Leaf and Twig 6X
    Thuja occidentalis (White cedar) Twig 8X
    Vanadium metallicum (Vanadium) 10X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with skin warts.

  • WARNINGS

    Warnings
    Stop use and ask a doctor if symptoms
    persist or worsen.
    If pregnant or breastfeeding, ask a
    health professional before use.
    Keep out of reach of children. In case
    of overdose, get medical help or contact
    a Poison Control Center right away.

  • 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.

  • PREGNANCY OR BREAST FEEDING

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

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.

  • INACTIVE INGREDIENT

    Inactive ingredients
    Ethanol (beet), purified water, lactose

  • DOSAGE & ADMINISTRATION

    Directions
    To be taken ten minutes away from
    food.
    Invert bottle and shake lightly allowing
    drops to fall directly under the tongue
    or into ¼ oz of water.
    Hold contents for about 20 seconds
    and swallow.
    To promote drop flow, invert bottle and
    shake before each use.

    Adults and adolescents (12 years and older)
    Take 10 drops two times daily, in the
    morning and evening, or as recommended
    by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your
    healthcare practitioner.

  • INDICATIONS & USAGE

    Uses
    For the temporary relief of symptoms associated with skin warts.

    Directions
    To be taken ten minutes away from
    food.
    Invert bottle and shake lightly allowing
    drops to fall directly under the tongue
    or into ¼ oz of water.
    Hold contents for about 20 seconds
    and swallow.
    To promote drop flow, invert bottle and
    shake before each use.

    Adults and adolescents (12 years and older)
    Take 10 drops two times daily, in the
    morning and evening, or as recommended
    by your healthcare practitioner.

    Children (under 12 years)

    Take under the direction of your
    healthcare practitioner.

  • PRINCIPAL DISPLAY PANEL

    62106-1238-8

    NDC 62106-1238-8

    UNDA

    plex

    ANTI-WART

    Homeopathic Preparation

    For the temporary relief of symptoms associated with skin warts.

    Contains 30% Alcohol

    0.7 fl oz (20 mL)

  • INGREDIENTS AND APPEARANCE
    ANTI-WART 
    bufo rana, buxus sempervirens, juglans regia, nitricum acidum, oleander, stannum metallicum, sulphur, taxus baccata, thuja occidentalis, vanadium metallicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1238
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN10 [hp_X]  in 20 mL
    ENGLISH WALNUT (UNII: 1V3SHR7QB7) (ENGLISH WALNUT - UNII:1V3SHR7QB7) ENGLISH WALNUT2 [hp_X]  in 20 mL
    NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (NERIUM OLEANDER LEAF - UNII:7KV510R6H6) NERIUM OLEANDER LEAF6 [hp_X]  in 20 mL
    BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (BUFO BUFO CUTANEOUS GLAND - UNII:Q59QU6N72Q) BUFO BUFO CUTANEOUS GLAND12 [hp_X]  in 20 mL
    NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID10 [hp_X]  in 20 mL
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR10 [hp_X]  in 20 mL
    THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG8 [hp_X]  in 20 mL
    VANADIUM (UNII: 00J9J9XKDE) (VANADIUM - UNII:00J9J9XKDE) VANADIUM10 [hp_X]  in 20 mL
    BUXUS SEMPERVIRENS LEAFY TWIG (UNII: L479H0RS38) (BUXUS SEMPERVIRENS LEAFY TWIG - UNII:L479H0RS38) BUXUS SEMPERVIRENS LEAFY TWIG6 [hp_X]  in 20 mL
    TAXUS BACCATA WHOLE (UNII: T0311VH21D) (TAXUS BACCATA WHOLE - UNII:T0311VH21D) TAXUS BACCATA WHOLE6 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1238-81 in 1 CARTON04/03/2017
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/03/2017
    Labeler - Seroyal USA (018361118)
    Establishment
    NameAddressID/FEIBusiness Operations
    SAN'UP401010287manufacture(62106-1238)