Label: DR HO S PAIN RELIEF EXTRA STGHT- methyl salicylate,menthol,eucalyptus oil cream

  • NDC Code(s): 71447-187-00, 71447-187-01
  • Packager: LABORATOIRES DRUIDE 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 February 8, 2023

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

  • DRUG FACTS

  • ACTIVE INGREDIENTS

    Methyl Salicylate 30%

    Menthol 15.00%

    Eucalyptus Oil 1%

  • Purpose

    Topical Analgesic

  • USES

    ■ Provides temporary soothing relief of sore muscles associated with strains and sprains, backaches, lumbago, pain of tendons and or ligaments as well as arthritic or rheumatic pain.

  • WARNINGS

    For external use only.

    ■ The application of external heat may cause skin irritation or burn.

    ■ Avoid contact with eyes and broken skin. Do not bandage.

    ■ DO NOT USE IF ALLERGIC TO SALICYLATES OR IF TAKING ANTICOAGULANT MEDICATIONS.

  • When using this product

    rashes and or burning discomfort have been known to occur; in which case discontinue use.

    ■ The application of external heat may cause skin irritation or burn.

  • Stop use and ask a doctor

    if condition worsens, rash or irritation develops, or if symptoms persist for more than 7 days or clear up and recur in a few days.

    ■ IF PREGNANT OF BREAST-FEEDING, ask a health professional before use.

  • Keep safely out of reach of children

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • DIRECTIONS

    ■ For use on adults and children over 12 years of age.

    ■ Apply generously to the affected area using hands-free applicator ■ Use 3 to 4 times per day as required. A stinging or burning sensation will be experienced during the first few minutes as the formula begins working. For arthritis or muscle pain of the hands, retain for at least 10 minutes then wash hands.

  • INACTIVE INGREDIENTS

    Paraffin wax, Butyrospermum Parkii (Shea) Butter, Cocos Nucifera (Coconut) Oil, Tocopherol.

  • Questions or Comments?

    1-877-374-6669 or visit www.drhonow.com

  • Distributed by

    VGH Solutions Inc
    150 Stewart Parkway
    Greensboro, GA 30642

    MADE IN CANADA

  • DR-HO'S PAIN RELIEF STICK EXTRA STRENGHT 1.86 OZ (53G) (NDC 71447-187-00)

    DR-HO'S PAIN RELIEF STICK EXTRA STRENGHT 1.86 OZ (53G)

  • INGREDIENTS AND APPEARANCE
    DR HO S PAIN RELIEF EXTRA STGHT 
    methyl salicylate,menthol,eucalyptus oil cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71447-187
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE30 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL15 g  in 100 g
    EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    COCOS NUCIFERA WHOLE (UNII: 245J88W96L)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71447-187-011 in 1 BOX02/08/2023
    1NDC:71447-187-0053 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34802/08/2023
    Labeler - LABORATOIRES DRUIDE INC (245815014)
    Registrant - LABORATOIRES DRUIDE INC (245815014)
    Establishment
    NameAddressID/FEIBusiness Operations
    LABORATOIRES DRUIDE INC245815014manufacture(71447-187)