Label: BLUE STAR MEDICATED- camphor ointment

  • NDC Code(s): 71687-2010-2
  • Packager: Focus Consumer Healthcare, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • Active Ingredient

    Camphor 1.24%

  • PURPOSE

    Purpose

    Toplcal Analgesic, Anti-itch

  • INDICATIONS & USAGE

    Use for temporarily relief of pain and itching associated with minor skin irritations.

  • WARNINGS

    Warnings

    For external use only

    When using this product avoid contact with eyes

    Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again with a few days

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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

  • DOSAGE & ADMINISTRATION

    • 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
  • INACTIVE INGREDIENT

    Benzoic acid, lanolin oil, methyl salicylate, mineral oil, parafin wax, petrolatum, salicylic acid, aloe oil extract

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    BLUE STAR MEDICATED 
    camphor ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71687-2010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)1.24 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN OIL (UNII: OVV5IIJ58F)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71687-2010-21 in 1 CARTON12/11/2017
    156 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/13/2017
    Labeler - Focus Consumer Healthcare, LLC (080743737)
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