EEZ-AWAY PAIN RELIEF (MENTHOL) LIQUID [EEZAWAY RELIEF INC]

EEZ-AWAY PAIN RELIEF (MENTHOL) LIQUID [EEZAWAY RELIEF INC]
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NDC 69678-111-02
Set ID da36730e-a684-4ba7-9d4d-013aceceb98b
Category HUMAN OTC DRUG LABEL
Packager EEZAWAY RELIEF INC
Generic Name
Product Class
Product Number
Application Number PART348
  • Drug Facts

  • Active ingredient:

    Menthol 2.50%

  • Purpose

    Topical Analgesic

  • Uses

    for temporary relief of minor aches and pains of muscles and joints associated with • bruises • sprains • arthritis • strains

  • Warnings:

    For external use only

    When using this product  

    Do not bandage tightly • avoid contact with eyes • do not apply to wounds or damaged skin • do not use with heating pads or other heating devices.

    Stop use and ask a doctor if

    • Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

  • Keep out of reach of children.

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

  • Directions

    • adults and children 12 years of age and older: apply to affected area no more than 10 times a day as needed for pain.

    • children under 12 years of age: do not use, consult a doctor.

  • Inactive ingredients:

    Isopropyl Alcohol, Deionized Water, PEG-75 Lanolin, Oleth-10, PPG-20 Methyl Glucose Ether, Iodine, Sodium Iodide, Ethyl Alcohol, Sodium Thiosulfate Pentahydrate, Fragrance.

  • QUESTIONS

    To reorder call:

    1-877 600 0016

  • SPL UNCLASSIFIED SECTION

    NEW! EXTRA STRENGTH ROLL-ON

    Recommended by

    • Top Physicians
    • Professional Athletes
    • Trainers

    Distributed exclusively by

    eez-Away Inc. P.O. Box 161, Hunterville, NC 28070

  • Packaging

    eez-label

  • INGREDIENTS AND APPEARANCE
    EEZ-AWAY PAIN RELIEF 
    menthol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69678-111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    POLYOXYL-10 OLEYL ETHER (UNII: JD797EF70J)  
    PPG-20 METHYL GLUCOSE ETHER (UNII: 3WV1T97D3K)  
    IODINE (UNII: 9679TC07X4)  
    SODIUM IODIDE (UNII: F5WR8N145C)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM THIOSULFATE (UNII: HX1032V43M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69678-111-0284 mL in 1 BOTTLE; Type 0: Not a Combination Product10/24/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34810/24/2018
    Labeler - EEZAWAY RELIEF INC (079751465)

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