Label: PLANTAR FASCIITIS CREAM- camphor cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 27, 2025

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  • ACTIVE INGREDIENT

    Camphor 5%

  • PURPOSE

    Topical Analgesic

  • INDICATIONS & USAGE

    - helps relieve minor foot and heel discomfort such as: arch tightness, stiffness, soreness linked to plantar fasciitis, ired or overused feet

  • WARNINGS

    For external use, do not take orally or get into eyes

    Do not use on open wounds.

    • if there are abnormalities such as skin rashes and allergies, do not scratch.
    • Avoid contact with eyes and mucous membranes

    If you experience an allergic reaction, discontinue use and consult a physician

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

  • DOSAGE & ADMINISTRATION

    • Clean the affected area before use.
    • Take an appropriate amount of this product and apply it evenly on the affected area, massage until completely absorbed.
    • Adults and children 12+, apply to affected area up to 3-4 times daily.
    • Children under 12, ask a doctor.
  • OTHER SAFETY INFORMATION

    Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

  • INACTIVE INGREDIENT

    Water, Glycerin, Angelica Sinensis Root, Taraxacum Officinale, Safflower, Black Pepper, Clove, Cinnamon, Cinnamomum Cassia Twig, Ligusticum Wallichii Root, Wormwood, Stearic Acid, Glyceryl Monostearate, Methylparaben, Phenoxyethanol, Borneol

  • QUESTIONS

    please contact us at: scogurei@gmail.com

  • PRINCIPAL DISPLAY PANEL

    cream

  • INGREDIENTS AND APPEARANCE
    PLANTAR FASCIITIS CREAM 
    camphor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85849-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR, (-)- (UNII: 213N3S8275) (CAMPHOR, (-)- - UNII:213N3S8275) CAMPHOR, (-)-50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ANGELICA SINENSIS ROOT (UNII: B66F4574UG)  
    TARAXACUM OFFICINALE (UNII: 39981FM375)  
    SAFFLOWER (UNII: 4VBL71TY4Y)  
    CLOVE (UNII: K48IKT5321)  
    CINNAMOMUM CASSIA TWIG (UNII: 4UD6VQR2UP)  
    WORMWOOD (UNII: F84709P2XV)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BORNEOL (UNII: M89NIB437X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)  
    BLACK PEPPER (UNII: KM66971LVF)  
    CINNAMON (UNII: 5S29HWU6QB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85849-012-0150 mL in 1 CARTON; Type 0: Not a Combination Product07/18/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/18/2025
    Labeler - SOLALIA LLC (060233478)
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