Label: BERBERIS PRUNUS 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 January 19, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • INDICATIONS & USAGE

    Under age 2: Consult a doctor.

  • DOSAGE & ADMINISTRATION

    Directions: Apply to skin in and around nose as needed.

  • ACTIVE INGREDIENT

    Active Ingredients: 100 gm contains: 50 gm Prunus spinosa (Blackthorn) 1X; Berberis (Barberry) 1X, Citrus (Lemon) 2X, Cydonia (Quince) 2X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Lanolin, Organic olive oil, Sunflower seed oil, Beeswax, Cajeput oil, Colloidal silica, Eucalyptus oil, Organic cane alcohol, Citric acid, Sorbic acid, Tea tree oil, Peruvian balsam, Grapefruit seed extract

    "prepared using rhythmical processes"

  • PURPOSE

    Use: Temporary relief of nasal congestion.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    KEEP OUT OF REACH OF CHILDREN
    Warnings: 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 on bag is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858
    Made with care by Uriel, East Troy, WI 53120
    shopuriel.com

  • PRINCIPAL DISPLAY PANEL

    Berberis Prunus Ointment

  • INGREDIENTS AND APPEARANCE
    BERBERIS PRUNUS 
    berberis prunus ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2148
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SLOE (UNII: 3MLB4858X7) (SLOE - UNII:3MLB4858X7) SLOE1 [hp_X]  in 1 g
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK1 [hp_X]  in 1 g
    LEMON (UNII: 24RS0A988O) (LEMON - UNII:24RS0A988O) LEMON2 [hp_X]  in 1 g
    QUINCE (UNII: 12MCS4H09N) (QUINCE - UNII:12MCS4H09N) QUINCE2 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CAJUPUT OIL (UNII: J3TO6BUQ37)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SORBIC ACID (UNII: X045WJ989B)  
    BALSAM PERU (UNII: 8P5F881OCY)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-2148-51 in 1 BAG09/01/2009
    110 g in 1 TUBE; Type 1: Convenience Kit of Co-Package
    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(48951-2148)
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!