Label: MEN-PHOR- menthol, camphor lotion

  • Category: HUMAN OTC DRUG LABEL

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 January 17, 2018

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  • Drug Facts

    Active Ingredients Purpose
    0.5% Camphor . . . .Anti-Infective, Anti-Pruritic
    0.5% Menthol . . . .Anti-Pruritic

  • Uses

    To provide temporary relief for dry
    itching skin, sunburn, insect bites and pruritus.

  • Directions

    • Apply two or three times daily, or as directed
    by your physician.

  • Warnings

    For External Use Only
    • Avoid contact with eyes. If contact occurs,
    rinse eyes thoroughly with water.
    • If improvement does not occur, or condition
    worsens after regular use as directed,
    discontinue use and consult a physician.
    • Do not use on children under two years of age.
    • Do not apply under compresses or bandages

  • Other Ingredient

    Alcohol, Carbomers, Cetyl Alcohol, DMDM Hydantoin, Fragrance, Glycerin, Glycol Stearate, Methylparaben, PEG-200 Dilaurate, PEG-40 Hydrogenated Castor Oil, Petrolatum, Propylparaben, Stearic Acid, Trolamine, Water

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • DOSAGE & ADMINISTRATION

    Apply two or three times daily.

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    MEN-PHOR 
    menthol, camphor lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54162-550
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.11 g  in 222 mL
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)1.11 g  in 222 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    PEG-200 DILAURATE (UNII: TWV5J70L88)  
    PEG-40 CASTOR OIL (UNII: 4ERD2076EF)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54162-550-07222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/31/2015
    2NDC:54162-550-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/2015
    3NDC:54162-550-09222 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product07/31/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34807/31/2015
    Labeler - Geritrex LLC (112796248)
    Establishment
    NameAddressID/FEIBusiness Operations
    Geritrex LLC112796248manufacture(54162-550)
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