Label: ROSE QUARTZ 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: Bryophyllum (Life plant) 2X, Rose quartz (Quartz colored rose-red by traces of manganese) 32X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Organic olive oil, Spring water, Beeswax, Lanolin, Sunflower seed oil, Sodium silicate, Lanolin alcohol, Citric acid, Geranium oil, Sorbic acid, Tea tree oil, Rose oil, Grapefruit seed extract

    Prepared using rhythmical processes.

  • PURPOSE

    Uses: Temporary relief and protection of dry, irritated skin and prevention of diaper rash.

  • 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

    rose Quartz Ointment

  • INGREDIENTS AND APPEARANCE
    ROSE QUARTZ 
    rose quartz ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8309
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE32 [hp_X]  in 1 g
    KALANCHOE DAIGREMONTIANA LEAF (UNII: L6X13JKL8O) (KALANCHOE DAIGREMONTIANA LEAF - UNII:L6X13JKL8O) KALANCHOE DAIGREMONTIANA LEAF2 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBIC ACID (UNII: X045WJ989B)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    WATER (UNII: 059QF0KO0R)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    LANOLIN (UNII: 7EV65EAW6H)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    SODIUM SILICATE (UNII: IJF18F77L3)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)  
    ROSE OIL (UNII: WUB68Y35M7)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8309-560 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(48951-8309)
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