Label: LYMPHASTAT F (echinacea (angustifolia), tabebuia impetiginosa, abies nigra, lycopodium clavatum, nux vomica, phosphorus, pulsatilla- vulgaris, sepia, skatolum, canadida albicans, 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 5, 2024

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  • ACTIVE INGREDIENTS:

    (in each drop): 12.48% of Abies Nigra 12X, Candida Albicans 30X, Lycopodium Clavatum 12X, Nux Vomica 12X, Phosphorus 12X, Pulsatilla (Vulgaris) 12X, Sepia 12X, Skatolum 15X; 0.10% of Echinacea (Angustifolia) 3X, Tabebuia Impetiginosa 3X.

  • INDICATIONS:

    May temporarily relieve symptoms associated with fungal conditions, such as heartburn and distention, burning on urination, flatulence, and apathy.**

    **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 fungal conditions, such as heartburn and distention, burning on urination, flatulence, and apathy.**

    **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

    LYMPHASTAT F

    1 fl. oz. (30 ml)

    LYMPHASTAT F

  • INGREDIENTS AND APPEARANCE
    LYMPHASTAT F 
    echinacea (angustifolia), tabebuia impetiginosa, abies nigra, lycopodium clavatum, nux vomica, phosphorus, pulsatilla (vulgaris), sepia, skatolum, canadida albicans, liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0605
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA WHOLE3 [hp_X]  in 1 mL
    TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX) (HANDROANTHUS IMPETIGINOSUS BARK - UNII:6GLA1946WX) TABEBUIA IMPETIGINOSA BARK3 [hp_X]  in 1 mL
    PICEA MARIANA RESIN (UNII: 71AOV0W131) (PICEA MARIANA RESIN - UNII:71AOV0W131) PICEA MARIANA RESIN12 [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
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS12 [hp_X]  in 1 mL
    PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) PULSATILLA VULGARIS WHOLE12 [hp_X]  in 1 mL
    SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE12 [hp_X]  in 1 mL
    SKATOLE (UNII: 9W945B5H7R) (SKATOLE - UNII:9W945B5H7R) SKATOLE15 [hp_X]  in 1 mL
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0605-130 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/25/202106/15/2027
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/25/202106/15/2027
    Labeler - Energique, Inc (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0605) , api manufacture(44911-0605) , label(44911-0605) , pack(44911-0605)
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