Label: NIGHTSHADE ANTIGENS (capsicum annuum, lycopersicum esculentum, solanum melongena, solanum tuberosum, tabacum, alumina, arsenicum album, nux vomica, phosphorus, pulsatilla- pratensis 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 20, 2020

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

  • ACTIVE INGREDIENTS:

    (in each drop): 3.44% of Alumina 12X, 15X, Arsenicum Album 12X, 15X, Capsicum Annuum 9X, 12X, 15X, 30X, Lycopersicum Esculentum 9X, 12X, 15X, 30X, Nux Vomica 12X, 15X, Phosphorus 12X, 15X, Pulsatilla (Pratensis) 12X, 15X, Solanum Melongena 12X, 15X, 30X, Solanum Tuberosum 9X, 12X, 15X, 30X, Tabacum 9X, 12X, 15X, 30X; 0.10% Solanum Melongena 9X.

  • INDICATIONS:

    May temporarily relieve symptoms associated with nightshade allergies.**

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

  • WARNINGS:

    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.

    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 nightshade 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
    NIGHTSHADE
    ANTIGENS
    1 fl. oz. (30 ml)

    Nightshade Antigens

    Nightshade Antigens

  • INGREDIENTS AND APPEARANCE
    NIGHTSHADE ANTIGENS 
    capsicum annuum, lycopersicum esculentum, solanum melongena, solanum tuberosum, tabacum, alumina, arsenicum album, nux vomica, phosphorus, pulsatilla (pratensis) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0350
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM9 [hp_X]  in 1 mL
    SOLANUM LYCOPERSICUM (UNII: 0243Q4990L) (SOLANUM LYCOPERSICUM - UNII:0243Q4990L) SOLANUM LYCOPERSICUM9 [hp_X]  in 1 mL
    EGGPLANT (UNII: W5K7RAS4VK) (EGGPLANT - UNII:W5K7RAS4VK) EGGPLANT9 [hp_X]  in 1 mL
    SOLANUM TUBEROSUM (UNII: 2A8I57T4MX) (SOLANUM TUBEROSUM - UNII:2A8I57T4MX) SOLANUM TUBEROSUM9 [hp_X]  in 1 mL
    TOBACCO LEAF (UNII: 6YR2608RSU) (TOBACCO LEAF - UNII:6YR2608RSU) TOBACCO LEAF9 [hp_X]  in 1 mL
    ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE12 [hp_X]  in 1 mL
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE12 [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
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS12 [hp_X]  in 1 mL
    ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0350-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product04/19/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/19/2016
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0350) , api manufacture(44911-0350) , label(44911-0350) , pack(44911-0350)