Label: QUALITY CHOICE CAMPHOR SPIRIT- camphor 10% liquid

  • NDC Code(s): 63868-490-02
  • Packager: Chain Drug Market Association
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2023

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

  • SPL UNCLASSIFIED SECTION


    Drug Facts

  • Active Ingredient

    Camphor 10%

  • Purpose

    External Anagesic

  • Indication

    For the temporary relief of minor aches, muscle and joint pain associated with arthritis, strains, brusies and simple backache.

  • Warnings

    For external use only.

    Do not drink. If swallowed, immediately give 3 or 4 glases of water. Do not induce vomiting. If vomiting occurs, give fluids again. Do not give anything by mouth to an unconscious or convulsing person. Get medical attention immediately.

    Avoid contact with eyes or mucous membranes.

    Do not apply to irritated skin.

    Do not use undiluted product.

  • When using this product

    Do not bandage tightly.

  • Discontinue use and consult a doctor if

    condition worsens, or if excesive irritation develops.

    symptoms persit for more than 7 days, or clear up and occur again within a few days.

  • Keep out of reach of children

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away. In case of eye contact, flush eyes with running water for 15 minutes, get medical attention.

  • Directions

    (dilute 3 parts olive oil and mix well)

    Adults and children 2 yrs. and older. apply to th affected area not more than 3 or 4 times daily.

    Children under 2 yrs of age: consult a doctor befre use.

  • Other Information

    Flammable: Keep away from spark, heat and flame.

  • Inactive ingredients

    Alcohol 84%, Purified Water

  • Principal Display Panel

    Camphor Spirits, USP

    label

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE CAMPHOR SPIRIT 
    camphor 10% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-490
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-490-02473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/12/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2008
    Labeler - Chain Drug Market Association (011920774)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(63868-490) , analysis(63868-490) , pack(63868-490) , label(63868-490)