Label: KATINKO PAIN AND ITCH RELIEVING (camphor- synthetic, menthol, methyl salicylate ointment

  • NDC Code(s): 52241-100-03, 52241-100-10, 52241-100-30
  • Packager: Greenstone Pharmaceutical Inc.
  • 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 August 11, 2021

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

  • ACTIVE INGREDIENT

    Active Ingredients:           

    Camphor 11 percent                 

    Menthol 7.6 percent                 

    Methyl Salicylate 13.0 percent  

  • Purpose

    Topical Analgesic

    Topical Analgesic

    Topical Analgesic

  • Uses:

    For temporary relief of minor aches and pains of muscles and joints associated with:

    Simple Backache       Arthritis      Rheumatism      Muscle Strain      Sprains      Bruises

    For temporary relief of pain and itching associated with:

    Insect Bites      Minor skin irritation

  • WARNINGS

    Warnings

    For External Use Only.

  • WHEN USING

    When using this product:

    Use only as directed.

    Do not apply to wounds or damaged skin.

    Do not use on the eyes or on the mucous membranes.

    Do not use with a heating pad or apply external heat.

  • STOP USE

    Stop use and ask a doctor if:

    Skin redness or excessive irritation of the skin occurs

    Condition worsens

    Symptoms persists for more than 7 days or clears up and occurs again within a few days

    Do not bandage tightly

  • Keep out of reach of children

    If swallowed, get medical help or contact a poison control

  • DOSAGE & ADMINISTRATION

    Directions:

    Adults and children 2 yrs and up              Apply to affected areas not more than 3 to 4 times daily

    Children under 2 years                             Consult a doctor before use

  • Other Information

    This product make provoke allergic reaction in some individuals. Test on small area before use.

  • Inactive Ingredients

    Petroleum Jelly, Paraffin Wax

  • MANUFACTURED BY:

    Greenstone

    Pharmaceutical

    H.K. Inc.

    Anabu Industrial Estate,

    Imus, Cavite, Philippines 4103

    PRODUCT O F THE PHI L I P PI N E S

    MEDICATED

    For external use only

  • PRINCIPAL DISPLAY PANEL

    10g stickers10g box

  • 30g Package Label

    30g Label

  • INGREDIENTS AND APPEARANCE
    KATINKO PAIN AND ITCH RELIEVING 
    camphor (synthetic), menthol, methyl salicylate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52241-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)11 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL7.6 g  in 100 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52241-100-101 in 1 CARTON05/24/2010
    110 g in 1 JAR; Type 0: Not a Combination Product
    2NDC:52241-100-031 in 1 CARTON05/24/2010
    23 g in 1 JAR; Type 0: Not a Combination Product
    3NDC:52241-100-301 in 1 CARTON05/24/2010
    330 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/24/2010
    Labeler - Greenstone Pharmaceutical Inc. (719794307)
    Registrant - Greenstone Pharmaceutical Inc. (719794307)
    Establishment
    NameAddressID/FEIBusiness Operations
    Greenstone Pharmaceutical Inc.719794307manufacture(52241-100)