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
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 9, 2020

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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)  
    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 not finalpart34810/13/2017
    Labeler - Focus Consumer Healthcare, LLC (080743737)