Label: ARTHRONEO- camphor spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 25, 2023

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  • Active Ingredient

    Camphor 0.50%

  • Purpose

    External Analgesic

  • Uses

    For temporary relief of pain

  • Warnings

    For external use only.

  • Do Not use

    In large quantities, particularly over raw surfaces or blistered areas.• If condition worsens or if symptoms persist for more than 7 days or clear up and ocur again within a few days, discontinue use of this product and consult a doctor.

  • When Using This Product

    Avoid contact with the eyes

  • Stop using and Ask a Doctor

    if irritation or rash occurs.

  • Keep Out Of Reach of Children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age:
    consult a doctor.

  • Other Information

    Keep dry. Store at 5'C and 20'C.

  • Inactive Ingredients

    Sensil CH SP, Amica montana flower extract, Benzyl alcohol, Citric acid, Disodium EDTA, Limonene, Lavandula angustifolia herb oil,
    Linalool, Peg-40 hydrogenated castor oil, Potassium sorbate, Propylene glycol, Sodium benzoate, Water

  • Principal Display

    Made in the EU

    Manufacturered for Likasso, LTD

    Grafenberger Alle 115

    4023 Dusseldorf, Germany

    NDC: 82312-001-50

    LABEL

    BOX

  • INGREDIENTS AND APPEARANCE
    ARTHRONEO 
    camphor spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82312-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    LINALOOL, (+)- (UNII: F4VNO44C09)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    PEG-40 CASTOR OIL (UNII: 4ERD2076EF)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82312-001-501 in 1 BOX10/27/2021
    150 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/27/2021
    Labeler - Likasso LTD (315086971)
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