Label: RET GALLBLADDER 7007- ret gallbladder 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

    Gorse flower essence 3X
    Rock water flower essence 3X
    Willow flower essence 3X
    Kali phosphoricum 3X, 6X, 30X
    and all the following at 30X, 100X, 200X:
    Cuprum metallicum
    Lachesis mutus
    Lycopodium clavatum
    Natrum muriaticum
    Stramonium

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    Temporarily relieves resentment, bitterness, self-pity, hopelessness, pessimism, self-perfection, dread, or anxiousness.*

  • 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 5 drops up to 4 times per day for up to one month. 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

    RET Gallbladder

    Homeopathic Remedy

    1 FL. OZ. (29.5 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    RET GALLBLADDER  7007
    ret gallbladder liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-7007
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN) (ULEX EUROPAEUS FLOWER - UNII:398DBS1PXN) ULEX EUROPAEUS FLOWER3 [hp_X]  in 29.5 mL
    ELEUTHEROCOCCUS SENTICOSUS ROOT OIL (UNII: 0DAF87OMMD) (ELEUTHEROCOCCUS SENTICOSUS ROOT OIL - UNII:0DAF87OMMD) ELEUTHEROCOCCUS SENTICOSUS ROOT OIL3 [hp_X]  in 29.5 mL
    SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (SALIX ALBA FLOWERING TOP - UNII:XBP5X7E70R) SALIX ALBA FLOWERING TOP3 [hp_X]  in 29.5 mL
    POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (POTASSIUM PHOSPHATE, UNSPECIFIED FORM - UNII:B7862WZ632) POTASSIUM PHOSPHATE, UNSPECIFIED FORM3 [hp_X]  in 29.5 mL
    COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER30 [hp_X]  in 29.5 mL
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM30 [hp_X]  in 29.5 mL
    LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE30 [hp_X]  in 29.5 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE30 [hp_X]  in 29.5 mL
    DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3) DATURA STRAMONIUM30 [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:63083-7007-129.5 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(63083-7007)
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!