Label: TARTARUS COMBINATION 9259- tartarus combination 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 August 15, 2019

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  • ACTIVE INGREDIENTS

    Stachys betonica 2X
    Anisum 3X
    Ephedra vulgaris 3X
    Hepatica triloba 3X
    Belladonna 4X
    Ipecacuanha 4X
    Lobelia inflata 4X
    Natrum sulphuricum 4X
    Quebracho 5X
    Antimonium tartaricum 6X
    Arsenicum iodatum 6X
    Blatta orientalis 6X
    Naphthalinum 6X
    Medorrhinum 12X
    Tuberculinum 12X

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of coughing, wheezing, nasal or bronchial congestion.*

  • PURPOSE

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

  • WARNINGS

    If symptoms do not improve or are accompanied by a fever, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

    Keep out of the reach of children.

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

  • DIRECTIONS

    Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

  • OTHER INFORMATION

    Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

  • INACTIVE INGREDIENTS

    40% ethanol, purified water.

  • LABEL

    Est 1985

    Professional Formulas

    Complementary Health

    Tartarus Combination

    Homeopathic Remedy

    1 FL. OZ. (29.5 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    TARTARUS COMBINATION  9259
    tartarus combination liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-9259
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N) STACHYS OFFICINALIS2 [hp_X]  in 29.5 mL
    ANISE (UNII: 21C2F5E8RE) (ANISE - UNII:21C2F5E8RE) ANISE3 [hp_X]  in 29.5 mL
    EPHEDRA DISTACHYA FLOWERING TWIG (UNII: R55VQ87DP3) (EPHEDRA DISTACHYA FLOWERING TWIG - UNII:R55VQ87DP3) EPHEDRA DISTACHYA FLOWERING TWIG3 [hp_X]  in 29.5 mL
    ANEMONE HEPATICA VAR. OBTUSA (UNII: 6ICN6T7FEM) (ANEMONE HEPATICA VAR. OBTUSA - UNII:6ICN6T7FEM) ANEMONE HEPATICA VAR. OBTUSA3 [hp_X]  in 29.5 mL
    AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (AMARYLLIS BELLADONNA WHOLE - UNII:11B89M58UN) AMARYLLIS BELLADONNA WHOLE4 [hp_X]  in 29.5 mL
    IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC4 [hp_X]  in 29.5 mL
    LOBELIA INFLATA WHOLE (UNII: 9PP1T3TC5U) (LOBELIA INFLATA WHOLE - UNII:9PP1T3TC5U) LOBELIA INFLATA WHOLE4 [hp_X]  in 29.5 mL
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE4 [hp_X]  in 29.5 mL
    ASPIDOSPERMA QUEBRACHO-BLANCO ROOT (UNII: 0MT70OWS53) (ASPIDOSPERMA QUEBRACHO-BLANCO ROOT - UNII:0MT70OWS53) ASPIDOSPERMA QUEBRACHO-BLANCO ROOT5 [hp_X]  in 29.5 mL
    ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE6 [hp_X]  in 29.5 mL
    ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIIODIDE6 [hp_X]  in 29.5 mL
    BLATTA ORIENTALIS (UNII: 535787266D) (BLATTA ORIENTALIS - UNII:535787266D) BLATTA ORIENTALIS6 [hp_X]  in 29.5 mL
    NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE6 [hp_X]  in 29.5 mL
    GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (GONORRHEAL URETHRAL SECRETION HUMAN - UNII:9BZG9E3I8F) GONORRHEAL URETHRAL SECRETION HUMAN12 [hp_X]  in 29.5 mL
    BOVINE TUBERCULIN (UNII: HKD62G79N5) (BOVINE TUBERCULIN - UNII:HKD62G79N5) BOVINE TUBERCULIN12 [hp_X]  in 29.5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63083-9259-129.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product08/15/1985
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/15/1984
    Labeler - Professional Complementary Health Formulas (167339027)
    Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natural Pharmaceutical Manufacturing LLC015624923manufacture(63083-9259)
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