Label: ANGINACID- apis mellifica, baryum muriaticum, belladonna, calcium iodatum, hepar sulphuris calcareum, kalium bichromicum, lachesis mutus, mercurius corrosivus, phytolacca decandra, teucrium marum verum liquid

  • 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 June 2, 2016

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredients
    Each drop contains:
    Apis mellifica (Honeybee) 4X
    Baryum muriaticum (Barium chloride) 6X
    Belladonna (Deadly nightshade) Whole Plant 4X (1 x 10-6% alkaloids, calculated)

    Calcium iodatum (Calcium iodide) 4X
    Hepar sulphuris calcareum (Crude calcium sulfide) 12X
    Kalium bichromicum (Potassium bichromate) 5X
    Lachesis mutus (Bushmaster) Venom 12X
    Mercurius corrosivus (Mercury (II) chloride) 8X
    Phytolacca decandra (Pokeweed) Root 4X
    Teucrium marum verum (Cat thyme) Aerial Parts 6X

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  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with minor local inflammation.

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  • 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.

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  • PREGNANCY OR BREAST FEEDING

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

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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  • OTHER SAFETY INFORMATION

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

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  • INACTIVE INGREDIENT

    Inactive ingredients
    Ethanol (beet), purified water

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  • 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.
    Dosage frequency may be increased up to six times daily depending on the severity of symptoms.

    Adults and adolescents (12 years and older)

    Take 10 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)
    Take under the direction of your healthcare practitioner.

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  • INDICATIONS & USAGE

    Uses
    For the temporary relief of symptoms associated with minor local inflammation.

    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.
    Dosage frequency may be increased up to six times daily depending on the severity of symptoms.

    Adults and adolescents (12 years and older)

    Take 10 drops three times daily or as recommended by your healthcare practitioner.

    Children (under 12 years)
    Take under the direction of your healthcare practitioner.

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  • PRINCIPAL DISPLAY PANEL

    NDC 62106-2024-0

    NDC 62106-2024-0

    UNDA

    vanocomplex

    1

    ANGINACID

    Homeopathic Preparation

    For the temporary relief of symptoms associated with minor local inflammation.

    Contains 31% Alcohol

    1.7 fl oz (50 ml)

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  • INGREDIENTS AND APPEARANCE
    ANGINACID 
    apis mellifica, baryum muriaticum, belladonna, calcium iodatum, hepar sulphuris calcareum, kalium bichromicum, lachesis mutus, mercurius corrosivus, phytolacca decandra, teucrium marum verum liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62106-2024
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA 4 [hp_X]  in 50 mL
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 12 [hp_X]  in 50 mL
    MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 8 [hp_X]  in 50 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 5 [hp_X]  in 50 mL
    TEUCRIUM MARUM (UNII: 10464S0TAA) (TEUCRIUM MARUM - UNII:10464S0TAA) TEUCRIUM MARUM 6 [hp_X]  in 50 mL
    PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG) PHYTOLACCA AMERICANA ROOT 4 [hp_X]  in 50 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 4 [hp_X]  in 50 mL
    BARIUM CHLORIDE (UNII: 0VK51DA1T2) (BARIUM CATION - UNII:V645272HLN) BARIUM CHLORIDE 6 [hp_X]  in 50 mL
    CALCIUM IODIDE (UNII: 8EKI9QEE2H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM IODIDE 4 [hp_X]  in 50 mL
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X]  in 50 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62106-2024-0 1 in 1 CARTON 06/02/2016
    1 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 06/02/2016
    Labeler - Seroyal USA (018361118)
    Establishment
    Name Address ID/FEI Business Operations
    Unda SA 400346069 manufacture(62106-2024)
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