Label: VAPORIZING COLDS RUB- menthol ointment

  • NDC Code(s): 61734-030-02, 61734-030-03, 61734-030-04, 61734-030-05
  • Packager: Delon Laboratories (1990) Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 5, 2023

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

  • Active ingredients

    Camphor 4.7%
    Eucalyptus oil 1.2%
    Menthol 2.6%


  • Purpose

    Cough suppressant & topical analgesic

    Cough suppressant

    Cough suppressant & topical analgesic

  • Uses

    temporarily relieves:

    • cough due to minor bronchial irritation associated with a cold or inhaled irritants
    • cough associated with a cold
    • minor aches and pains of muscles and joints
  • Warnings

    For external use only; avoid contact with eyes.

    Do not use:

    • by mouth
    • on wounds or damaged skin
    • in nostrils
    • with tight bandages

    Ask a doctor before use if you have

    • excessive phlegm (mucus)
    • emphysema
    • persistent or chronic cough
    • asthma
    • cough associated with smoking

    When using this product, do not

    • heat
    • microwave
    • add to hot water or any container where heating water. May cause splattering and result in burns.

    Stop use and ask a doctor if

    • muscle aches and pains worsen or persist for more than 7 days or clear up and occur again within a few days
    • cough perists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center​ right away.

  • Directions

    • see important warnings under "When using this product"
    • adults and children 2 years and older:
    • rub on the throat and chest in a thick layer
    • cover with a warm, dry cloth if desired
    • clothing should be loose about throat and chest to help vapors reach the nose and mouth
    • use up to three times daily or as directed by a doctor
    • children under 2 years of age: ask a doctor
  • Other information

    • store at room temperature
  • Inactive ingredients

    cedar leaf oil, petrolatum, thymol, turpentine

  • Penetro 1.75oz

    Penetro Vaporizing Medicated  Rub 1.75oz BoxPenetro Vaporizing Medicated Rub 1.75oz label

  • Delon 4oz (113g)

    Delon Vaporizing Colds Rub 113g

  • Penetro 4oz

    Penetro Vaporizing Medicated Rub 4oz boxPenetro Vaporizing Medicated Rub 4oz label

  • INGREDIENTS AND APPEARANCE
    VAPORIZING COLDS RUB 
    menthol ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.6 g  in 100 g
    EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL1.2 g  in 100 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)4.73 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    CEDAR LEAF OIL (UNII: BJ169U4NLG)  
    THYMOL (UNII: 3J50XA376E)  
    TURPENTINE (UNII: XJ6RUH0O4G)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61734-030-0490 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/24/201112/04/2014
    2NDC:61734-030-02113 g in 1 JAR; Type 0: Not a Combination Product05/24/2011
    3NDC:61734-030-0350 g in 1 JAR; Type 0: Not a Combination Product05/24/2011
    4NDC:61734-030-0585 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/22/201810/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/24/2011
    Labeler - Delon Laboratories (1990) Ltd (248364184)
    Establishment
    NameAddressID/FEIBusiness Operations
    Laboratoires Delon208896216label(61734-030) , manufacture(61734-030) , pack(61734-030)