Label: ARNICA HYPERICUM DKS SPECIAL ORDER 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 June 25, 2019

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

  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY.

  • DOSAGE & ADMINISTRATION

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

  • ACTIVE INGREDIENT

    Active Ingredients: Hypericum (St. John’s Wort) 5X/10X, Aconitum (Monkshood) 6X, Aurum met. (Metallic gold) 6X, Oxalis (Wood sorrel) 6X, Stibium met. (Antimony) 6X, Urtica dioica (Stinging nettle) 6X, Arnica 6X/12X, Granite (Primitive rock containing quartz, feldspar, mica) 12X, Rosa (Garden rose) 6X/15X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Organic olive oil, Lanolin, Beeswax, Distilled water, Sunflower seed oil, Tea tree oil, Grapefruit seed extract, Lactose

  • PURPOSE

    Use: Temporary relief of headache.

  • 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. Contains traces of lactose. 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
    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    Arnica Hypericum DKS Special Order Ointment

  • INGREDIENTS AND APPEARANCE
    ARNICA HYPERICUM DKS SPECIAL ORDER 
    arnica hypericum dks special order ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1304
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS6 [hp_X]  in 1 g
    URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46) URTICA DIOICA6 [hp_X]  in 1 g
    ST. JOHN'S WORT (UNII: UFH8805FKA) (ST. JOHN'S WORT - UNII:UFH8805FKA) ST. JOHN'S WORT5 [hp_X]  in 1 g
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD6 [hp_X]  in 1 g
    OXALIS STRICTA WHOLE (UNII: 3STW243384) (OXALIS STRICTA WHOLE - UNII:3STW243384) OXALIS STRICTA WHOLE6 [hp_X]  in 1 g
    SEDUM ROSEUM WHOLE (UNII: RH0WP583U3) (SEDUM ROSEUM WHOLE - UNII:RH0WP583U3) SEDUM ROSEUM WHOLE6 [hp_X]  in 1 g
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ) ARNICA MONTANA FLOWER6 [hp_X]  in 1 g
    PENOXSULAM (UNII: 784ELC1SCZ) (PENOXSULAM - UNII:784ELC1SCZ) PENOXSULAM12 [hp_X]  in 1 g
    ANTIMONY (UNII: 9IT35J3UV3) (ANTIMONY - UNII:9IT35J3UV3) ANTIMONY6 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    WATER (UNII: 059QF0KO0R)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    LANOLIN (UNII: 7EV65EAW6H)  
    SORBIC ACID (UNII: X045WJ989B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1304-560 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(48951-1304)