Label: OXALIS 5- oxalis montana leaf cream

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

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 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 (UNII: U1W3U02EW0) (OXALIS MONTANA LEAF - UNII:U1W3U02EW0) OXALIS MONTANA LEAF 5 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    FRANKINCENSE OIL (UNII: 67ZYA5T02K)  
    MYRRH OIL (UNII: H74221J5J4)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    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