Label: ALCOSTAT- beta vulgaris, taraxacum officinale, trifolium pratense, capsicum annuum, chelidonium majus, lycopodium clavatum, nox vomica, quercus glandium spiritus, sulphuricum acidum, ethylicum, saccharum officinale, 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 March 8, 2022

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  • ACTIVE INGREDIENTS:

    (in each drop): 11.08% of Capsicum Annuum 12X, Chelidonium Majus 12X, Ethylicum 12X, 30X, Lycopodium Clavatum 12X, Nux Vomica 12X, Quercus Glandium Spiritus 12X, Saccharum Officinale 30X, Sulphuricum Acidum 12X; 0.10% of Beta Vulgaris 3X, Taraxacum Officinale 3X, Trifolium Pratense 3X.

  • INDICATIONS:

    May temporarily relieve loss of appetite, stomach upset, nausea, and craving of alcohol.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • WARNINGS:

    If pregnant or breast-feeding, 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.

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

  • 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.

  • DIRECTIONS:

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    May temporarily relieve loss of appetite, stomach upset, nausea, and craving of alcohol.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • INACTIVE INGREDIENTS:

    Demineralized water, 20% Ethanol.

  • QUESTIONS:

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579   800.869.8078

  • PACKAGE LABEL DISPLAY:

    ENERGIQUE

    SINCE 1987

    HOMEOPATHIC REMEDY

    ALCOSTAT

    1 fl. oz. (30 ml)

    ALCOSTAT

  • INGREDIENTS AND APPEARANCE
    ALCOSTAT 
    beta vulgaris, taraxacum officinale, trifolium pratense, capsicum annuum, chelidonium majus, lycopodium clavatum, nox vomica, quercus glandium spiritus, sulphuricum acidum, ethylicum, saccharum officinale, liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0182
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETA VULGARIS WHOLE (UNII: 4G174V5051) (BETA VULGARIS WHOLE - UNII:4G174V5051) BETA VULGARIS WHOLE3 [hp_X]  in 1 mL
    TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE3 [hp_X]  in 1 mL
    TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (TRIFOLIUM PRATENSE FLOWER - UNII:4JS0838828) TRIFOLIUM PRATENSE FLOWER3 [hp_X]  in 1 mL
    CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM12 [hp_X]  in 1 mL
    CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS WHOLE - UNII:7E889U5RNN) CHELIDONIUM MAJUS WHOLE12 [hp_X]  in 1 mL
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE12 [hp_X]  in 1 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED12 [hp_X]  in 1 mL
    QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY) (QUERCUS ROBUR NUT - UNII:Q7MU1F4GLY) QUERCUS ROBUR NUT12 [hp_X]  in 1 mL
    SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID12 [hp_X]  in 1 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL12 [hp_X]  in 1 mL
    SUCROSE (UNII: C151H8M554) (SUCROSE - UNII:C151H8M554) SUCROSE30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0182-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/05/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/08/2015
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0182) , api manufacture(44911-0182) , label(44911-0182) , pack(44911-0182)
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