Label: SUSTAFIX- camphor cream

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

Drug Label Information

Updated October 25, 2023

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

  • Active Ingredient

    Camphor 1.00%

  • Purpose

    External Analgesic

  • Uses

    For temporary relief of pain

  • Warnings

    For external use only. Contains bee venom.

  • 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 15°C and 30°C. Avoid direct sunlight.

  • Inactive Ingredients

    Acetylated glycol stearate, Aesculus hippocastanum extract, Amica montana flower extract, Beezwax, Benehyl alcohol, Butyrospermum parkii butter, Ceteth-251 Cet:yl alcohol, Cyclopentasiloxane, Dimethicone, Ethylhexylglycerin, Ethylhexyl stearate, EucalypbJs globulus leaf oil, Harpagophytum procumbens root extract, Limonen, Linalool, PEG-9 stearate, Phenoxyethanol, Propolis extract, Propylene glycol, Rosmarinus officianalis leaf oil, Sesamum indicum seed oil, Sodium polyacrylate, Trideceth-61 Water, Bee venom, BHT1 Methyl nicotinate

  • Principal Display

    Made in the EU

    Manufacturered for Likasso, LTD

    Grafenberger Alle 115

    4023 Dusseldorf, Germany

    NDC: 82312-002-10

    tube

    box

  • INGREDIENTS AND APPEARANCE
    SUSTAFIX 
    camphor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82312-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)  
    CETETH-25 (UNII: 5KLY4IOG20)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    LINALOOL, (+)- (UNII: F4VNO44C09)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    WATER (UNII: 059QF0KO0R)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    APIS MELLIFERA VENOM (UNII: 76013O881M)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    METHYL NICOTINATE (UNII: 7B1AVU9DJN)  
    PEG-9 STEARATE (UNII: WZU67V0H4I)  
    HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    SESAMUM INDICUM WHOLE (UNII: JD6YPE8XLT)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82312-002-101 in 1 BOX10/27/2021
    1100 g in 1 TUBE; 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)