Label: OXALIS 20% cream

  • 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 May 13, 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 Ingredient: 100 gm contains: 20 gm Oxalis (Wood sorrel) 1X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Spring water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Sorbic acid, Tea tree oil, Frankincense oil, Grapefruit seed extract, Myrrh oil

    "prepared using rhythmical processes"

  • PURPOSE

    Use: Temporary relief of cramps.

  • 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, Easy Troy, WI 53120
    shopuriel.com Lot#

  • PRINCIPAL DISPLAY PANEL

    Oxalis 20 Cream

  • INGREDIENTS AND APPEARANCE
    OXALIS 20% 
    oxalis 20% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7198
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXALIS STRICTA WHOLE (UNII: 3STW243384) (OXALIS STRICTA WHOLE - UNII:3STW243384) OXALIS STRICTA WHOLE1 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    SORBIC ACID (UNII: X045WJ989B)  
    FRANKINCENSE OIL (UNII: 67ZYA5T02K)  
    WATER (UNII: 059QF0KO0R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    MYRRH OIL (UNII: H74221J5J4)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-7198-560 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
    Oxalis 20%043471163manufacture(48951-7198)
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