Label: OXALIS 5- oxalis montana leaf cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 11/13

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

  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY.

    Close
  • DOSAGE & ADMINISTRATION

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

    Close
  • ACTIVE INGREDIENT

    Active Ingredient: Oxalis e pl. tota 3X

    Close
  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Potassium sorbate, Frankincense oil, Myrrh oil, Grapefruit seed extract

    Close
  • PURPOSE

    Use: Temporary relief of cramps.

    Close
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

    Close
  • WARNINGS

    Warnings: FOR EXTERNAL USE ONLY.
    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. Natural ingredients may cause color and/or scent variation.

    Close
  • QUESTIONS

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

    Close
  • INGREDIENTS AND APPEARANCE
    OXALIS 5 
    oxalis 5 cream
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:48951-7106
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OXALIS MONTANA LEAF (OXALIS MONTANA LEAF) OXALIS MONTANA LEAF 5 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    STEARIC ACID  
    ISOPROPYL MYRISTATE  
    LAVENDER OIL  
    CETYL ALCOHOL  
    POLYOXYL 40 STEARATE  
    STEARYL ALCOHOL  
    XANTHAN GUM  
    POTASSIUM SORBATE  
    FRANKINCENSE OIL  
    MYRRH OIL  
    CITRUS PARADISI SEED  
    Product Characteristics
    Color white Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-7106-5 60 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    Uriel Pharmacy Inc. 043471163 manufacture(48951-7106)
    Close