Label: CLEMATIS COMBINATION 9219- clematis 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

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

View All Sections
  • ACTIVE INGREDIENTS

    Betula alba 2X
    Caltha palustris 3X
    Galium aparine 3X
    Sedum acre 3X
    Thuja occidentalis 3X
    Urtica urens 3X
    Clematis erecta 4X
    Hedera helix 4X
    Juniperus communis 4X
    Ononis spinosa 4X
    Quillaja saponaria 4X
    Sempervivum tectorum 4X
    Echinacea angustifolia 5X
    Calcarea fluorica 6X
    Nitricum acidum 6X
    Argentum metallicum 8X
    Phosphorus 8X
    Apis mellifica 12X
    Pyrogenium 12X

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of minor aches, swelling, pain, or tingling of the joints, muscles, or extremities.*

  • PURPOSE

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

  • WARNINGS

    In case of overdose, get medical help or contact a poison control center right away.

    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

    Clematis Combination

    Homeopathic Remedy

    1 FL. OZ. (29.5 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    CLEMATIS COMBINATION  9219
    clematis combination liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-9219
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BETULA PUBESCENS WHOLE (UNII: 154QC2322L) (BETULA PUBESCENS WHOLE - UNII:154QC2322L) BETULA PUBESCENS WHOLE2 [hp_X]  in 29.5 mL
    CALTHA PALUSTRIS WHOLE (UNII: 6S9317F2UT) (CALTHA PALUSTRIS WHOLE - UNII:6S9317F2UT) CALTHA PALUSTRIS WHOLE3 [hp_X]  in 29.5 mL
    GALIUM APARINE WHOLE (UNII: Z4B6561488) (GALIUM APARINE WHOLE - UNII:Z4B6561488) GALIUM APARINE WHOLE3 [hp_X]  in 29.5 mL
    SEDUM ACRE WHOLE (UNII: 2496VW6S9J) (SEDUM ACRE WHOLE - UNII:2496VW6S9J) SEDUM ACRE WHOLE3 [hp_X]  in 29.5 mL
    THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786) THUJA OCCIDENTALIS LEAF3 [hp_X]  in 29.5 mL
    URTICA URENS WHOLE (UNII: IHN2NQ5OF9) (URTICA URENS WHOLE - UNII:IHN2NQ5OF9) URTICA URENS WHOLE3 [hp_X]  in 29.5 mL
    CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (CLEMATIS RECTA FLOWERING TOP - UNII:396421SP9F) CLEMATIS RECTA FLOWERING TOP4 [hp_X]  in 29.5 mL
    HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM) (HEDERA HELIX FLOWERING TWIG - UNII:3D10KUA6BM) HEDERA HELIX FLOWERING TWIG4 [hp_X]  in 29.5 mL
    JUNIPERUS COMMUNIS VAR. SAXATILIS WHOLE (UNII: 360QM23QBR) (JUNIPERUS COMMUNIS VAR. SAXATILIS WHOLE - UNII:360QM23QBR) JUNIPERUS COMMUNIS VAR. SAXATILIS WHOLE4 [hp_X]  in 29.5 mL
    ONONIS REPENS WHOLE (UNII: 7J37EHM6J6) (ONONIS REPENS WHOLE - UNII:7J37EHM6J6) ONONIS REPENS WHOLE4 [hp_X]  in 29.5 mL
    QUILLAJA SAPONARIA WOOD (UNII: 1L8K0593B6) (QUILLAJA SAPONARIA WOOD - UNII:1L8K0593B6) QUILLAJA SAPONARIA WOOD4 [hp_X]  in 29.5 mL
    SEMPERVIVUM TECTORUM LEAF (UNII: 3DGJ7BUA01) (SEMPERVIVUM TECTORUM LEAF - UNII:3DGJ7BUA01) SEMPERVIVUM TECTORUM LEAF4 [hp_X]  in 29.5 mL
    ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA WHOLE - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA WHOLE5 [hp_X]  in 29.5 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE6 [hp_X]  in 29.5 mL
    NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID6 [hp_X]  in 29.5 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER8 [hp_X]  in 29.5 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS8 [hp_X]  in 29.5 mL
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA12 [hp_X]  in 29.5 mL
    RANCID BEEF (UNII: 29SUH5R3HU) (RANCID BEEF - UNII:29SUH5R3HU) RANCID BEEF12 [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:63083-9219-129.5 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(63083-9219)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!