Label: PLANTAIN BEESWAX MILD 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 November 15, 2024

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  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Apply to the chest, back and soles of feet in the morning and evening or as needed, and cover warmly. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: 100 gm contains: 50 gm Resina laricis (Larch resin) 1X; Salvia (Sage) 3X, Drosera (Sundew) 4X, Petasites (Butterbur) 4X, Plantago (Ribwort plantain) 4X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Organic olive oil, Distilled water, Beeswax, Lanolin, Camphor, Glycerin, Sodium alginate, Sorbic acid, Tea tree oil, Grapefruit seed extract

    Prepared using rhythmical processes.

  • PURPOSE

    Uses: Temporary relief of cough and chest congestion.

  • 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

    Plantain Beeswax Mild Ointment

  • INGREDIENTS AND APPEARANCE
    PLANTAIN BEESWAX MILD 
    plantain beeswax mild ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8355
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PETASITES HYBRIDUS ROOT (UNII: 97S2809V5R) (PETASITES HYBRIDUS ROOT - UNII:97S2809V5R) PETASITES HYBRIDUS ROOT4 [hp_X]  in 1 g
    PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X) PLANTAGO MAJOR LEAF4 [hp_X]  in 1 g
    LARIX DECIDUA RESIN (UNII: AD8LJ73GQF) (LARIX DECIDUA RESIN - UNII:AD8LJ73GQF) LARIX DECIDUA RESIN1 [hp_X]  in 1 g
    SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE3 [hp_X]  in 1 g
    DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA4 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    WATER (UNII: 059QF0KO0R)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    LANOLIN (UNII: 7EV65EAW6H)  
    SORBIC ACID (UNII: X045WJ989B)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8355-560 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(48951-8355)
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