Label: CONNECTIVE TISSUE LIQUESCENCE 3024- connective tissue liquescence 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

    Collagen 3X
    Hypericum perforatum 3X
    Ligament 3X
    Ruta graveolens 3X
    Synovium 3X
    Bryonia 4X
    Arnica montana 6X
    Bone marrow 6X
    Chondroitin sulfate 6X
    Eupatorium perfoliatum 6X
    Glucosamine sulfate 6X
    Magnesium metallicum 6X
    Manganum metallicum 6X
    Rhus toxicodendron 6X
    Silicea 6X

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of minor aches and pains in the bones, muscles, or joints.*

  • 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 one full dropper up to 2 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

    20% ethanol, purified water.

  • LABEL

    Est 1985

    Professional Formulas

    Complementary Health

    Connective Tissue Liquescence

    Homeopathic Remedy

    4 FL. OZ. (118 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    CONNECTIVE TISSUE LIQUESCENCE  3024
    connective tissue liquescence liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-3024
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOVINE TYPE I COLLAGEN (SKIN) (UNII: 0127KU7397) (BOVINE TYPE I COLLAGEN (SKIN) - UNII:0127KU7397) BOVINE TYPE I COLLAGEN (SKIN)3 [hp_X]  in 118 mL
    HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM WHOLE - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM WHOLE3 [hp_X]  in 118 mL
    BOS TAURUS LIGAMENT (UNII: 0O005HD2J8) (BOS TAURUS LIGAMENT - UNII:0O005HD2J8) BOS TAURUS LIGAMENT3 [hp_X]  in 118 mL
    RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP3 [hp_X]  in 118 mL
    BOS TAURUS NERVE (UNII: 28G2U3MQJK) (BOS TAURUS NERVE - UNII:28G2U3MQJK) BOS TAURUS NERVE3 [hp_X]  in 118 mL
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT4 [hp_X]  in 118 mL
    ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW) ARNICA MONTANA WHOLE6 [hp_X]  in 118 mL
    BOS TAURUS BONE MARROW (UNII: 08X0K2M57P) (BOS TAURUS BONE MARROW - UNII:08X0K2M57P) BOS TAURUS BONE MARROW6 [hp_X]  in 118 mL
    CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z) (CONDOLIASE - UNII:7SI2UZG934) CHONDROITIN SULFATE (BOVINE)6 [hp_X]  in 118 mL
    EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP6 [hp_X]  in 118 mL
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) (GLUCOSAMINE - UNII:N08U5BOQ1K) GLUCOSAMINE SULFATE6 [hp_X]  in 118 mL
    MAGNESIUM (UNII: I38ZP9992A) (MAGNESIUM - UNII:I38ZP9992A) MAGNESIUM6 [hp_X]  in 118 mL
    MANGANESE (UNII: 42Z2K6ZL8P) (MANGANESE - UNII:42Z2K6ZL8P) MANGANESE6 [hp_X]  in 118 mL
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF6 [hp_X]  in 118 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 [hp_X]  in 118 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63083-3024-4118 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(63083-3024)
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