Label: EUCALYPTUS COMP. ointment

  • 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 December 11, 2024

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  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Apply to skin as needed. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Drosera (Sundew) 1X, Petasites (Butterbur) 1X, Plantago (Ribwort plantain) 1X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Organic olive oil, Beeswax, Lanolin, Spring water, Larch resin, Sunflower seed oil, Distilled water, Eucalyptus oil, Lavender oil, Thyme oil, Sorbic acid, Tea tree oil, Grapefruit seed extract

    Prepared using rhythmical processes.

  • PURPOSE

    Use: Temporary relief of flu symptoms.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: FOR EXTERNAL USE ONLY.
    Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858

    Made with care by Uriel, East Troy, WI 53120

    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Eucalyptus comp. Ointment

  • INGREDIENTS AND APPEARANCE
    EUCALYPTUS COMP. 
    eucalyptus comp. ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-4194
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA1 [hp_X]  in 1 g
    PETASITES HYBRIDUS ROOT (UNII: 97S2809V5R) (PETASITES HYBRIDUS ROOT - UNII:97S2809V5R) PETASITES HYBRIDUS ROOT1 [hp_X]  in 1 g
    PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X) PLANTAGO MAJOR LEAF1 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    LANOLIN (UNII: 7EV65EAW6H)  
    WATER (UNII: 059QF0KO0R)  
    LARIX DECIDUA RESIN (UNII: AD8LJ73GQF)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    THYME OIL (UNII: 2UK410MY6B)  
    SORBIC ACID (UNII: X045WJ989B)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-4194-560 g in 1 TUBE; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-4194)
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