Label: COFFEE TEA CHOCOLATE ANTIGENS (lycopodium clavatum, causticum, kali bichromicum, nux vomica, oxalicum acidum, pulsatilla- pratensis, sepia, cacao, coffea cruda thea sinensis 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 April 11, 2019

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

  • ACTIVE INGREDIENTS:

    (in each drop): 3.84% of Cacao 13X, 15X, 18X, 33X, Causticum 12X, 15X, Coffea Cruda 13X, 15X, 18X, 33X, Kali Bichromicum 12X, 15X, Lycopodium Clavatum 12X, 15X, Nux Vomica 12X, 15X, Oxalicum Acidum 12X, 15X, Pulsatilla (Pratensis) 12X, 15X, Sepia 12X, 15X, Thea Sinensis 13X, 15X, 18X, 33X; 0.10% of Lycopodium Clavatum 3X.

  • INDICATIONS:

    May temporarily relieve symptoms associated with coffee, tea, and chocolate allergies.**

    **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 symptoms associated with coffee, tea, and chocolate allergies.**

    **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

    COFFEE/TEA/

    CHOCOLATE

    ANTIGENS

    1 fl. oz. (30 ml)

    COFFEE TEA CHOCOLATE ANTIGENS

  • INGREDIENTS AND APPEARANCE
    COFFEE TEA CHOCOLATE ANTIGENS 
    lycopodium clavatum, causticum, kali bichromicum, nux vomica, oxalicum acidum, pulsatilla (pratensis), sepia, cacao, coffea cruda thea sinensis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0220
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE3 [hp_X]  in 1 mL
    CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM12 [hp_X]  in 1 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE12 [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
    OXALIC ACID (UNII: 9E7R5L6H31) (OXALIC ACID - UNII:9E7R5L6H31) OXALIC ACID12 [hp_X]  in 1 mL
    PULSATILLA PRATENSIS (UNII: 8E272251DI) (PULSATILLA PRATENSIS - UNII:8E272251DI) PULSATILLA PRATENSIS12 [hp_X]  in 1 mL
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE12 [hp_X]  in 1 mL
    COCOA (UNII: D9108TZ9KG) (COCOA - UNII:D9108TZ9KG) COCOA13 [hp_X]  in 1 mL
    ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72) ARABICA COFFEE BEAN13 [hp_X]  in 1 mL
    GREEN TEA LEAF (UNII: W2ZU1RY8B0) (GREEN TEA LEAF - UNII:W2ZU1RY8B0) GREEN TEA LEAF13 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0220-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/15/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/15/2015
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0220) , api manufacture(44911-0220) , label(44911-0220) , pack(44911-0220)