Label: DOCTOR HOYS PAIN RELIEF GEL (menthol, camphor- synthetic gel

  • NDC Code(s): 75638-010-00, 75638-010-01, 75638-010-02, 75638-010-03
  • Packager: Dynamic Blending Specialists, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 21, 2023

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  • Drug Facts:

  • Active ingredients:

    Menthol (5%)

    Camphor (5%)

    Purpose:

    Topical Analgesic

  • Uses:

    Temporary relief of minor aches and pains of muscles and joints due to: simple backache • arthritis • sprains • strains 

  • Warnings:

    • For external use only

    • Use as directed 

    • Avoid contact with eyes or mucus membranes

    • Do not apply to open wounds, irritated or damaged skin

    Keep Out of reach of children

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

    If pregnant or breast feeding,

    • ask a health professional before use

    • Discontinue use of this product and consult a physician if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days 

    • Use caution with wrap or heating pad.

  • Directions:

    For adults and children 2 years and older: For best results, shake well and apply generously. Use 1 layer for minor pain, 2 layers for medium and 3 layers for severe symptoms • Rub in well and allow to dry between layers (usually 2-3 minutes) • Repeat process up to 4 times daily • for children under 2 years of age: Consult a physician before use.

  • Inactive ingedients:

    Alcohol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Arnica Montana (Arnica Flower) Extract, Biosaccharide Gum-1, Butyrospermum Parkii (Shea) Butter Extract, Ethylhexylglycerin, Euphorbia Cerifera (Candelilla) Wax, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Hydrated Silica, Jojoba Esters, Phenoxyethanol, Polyglyceryl-10 Caprylate/Caprate, SD Alcohol 40-B, Sodium Starch Octenylsuccinate, Tocopherol Acetate, Water, Zanthoxylum Bungeanum Fruit Extract.

  • 75638-010-00

    Label89ml

  • 75638-010-01

    Label177ml

  • 75638-010-02

    Label946ml

  • 75638-010-03

    Label1893ml

  • INGREDIENTS AND APPEARANCE
    DOCTOR HOYS PAIN RELIEF GEL 
    menthol, camphor (synthetic) gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75638-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL50 mg  in 1 mL
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    ARNICA MONTANA WHOLE (UNII: O80TY208ZW)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    ZANTHOXYLUM BUNGEANUM FRUIT (UNII: 3CIP16A418)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75638-010-0089 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
    2NDC:75638-010-01177 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
    3NDC:75638-010-02946 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
    4NDC:75638-010-031893 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/2023
    Labeler - Dynamic Blending Specialists, Inc. (085704438)
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