PAIN RELIEF (ANALGESIC MENTHOL) SPRAY [UNIFIRST FIRST AID CORPORATION]

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PAIN RELIEF (ANALGESIC MENTHOL) SPRAY [UNIFIRST FIRST AID CORPORATION]
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NDC 47682-321-02
Set ID 8162d22d-04c0-de07-e053-2991aa0a9975
Category HUMAN OTC DRUG LABEL
Packager Unifirst First Aid Corporation
Generic Name
Product Class
Product Number
Application Number PART348
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  • Drug Facts

  • Active ingredients

    USP Menthol 7%

  • Purpose

    Topical analgesic

  • Uses

    Temporary relief of minor aches and pains of muscles and joints.

  • Warnings

    For external use only. Flammable. Keep away from flame.

    Do not use

    • on open wounds or damaged skin

    Ask a doctor before use if

    • you are prone to allergic reactions to salicylates, including aspirin

    When using this product

    • avoid contact with eyes

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clear up and recur again within a few days
    • excessive skin irritation occurs
  • If pregnant or breast feeding,

    ask a doctor before use.

  • Keep out of reach of children.

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

  • Directions

    Adults and children (2 years and older):

    Shake well and aply to affected araea not more than 3-4 times daily.

    Do not bandage tightly.

    Children under 2 years:

    Consult a doctor

  • Other information

    • store at room temperature 56°-86°F (15°-30°C)
    • will not stain clothing
  • Inactive ingredients

    coconut oil, eucalyptus lkeaf oil, glycerol, isopropyl alcohol, peppermint oil, water, wintergreen leaf oil

  • Questions or comments?

    1-800-869-6970

  • Green Guard Pain Relief Spray Label

    Pain Relief spray

    Fast Acting pain Relief

    For Temporary Relief of Minor Aches and Pains

    Green Guard®

    2 Fl. Oz. (59.1 mL)

    Green Guard

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEF 
    analgesic menthol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-321
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL70 mg  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-321-020.059 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34804/01/2019
    Labeler - Unifirst First Aid Corporation (832947092)
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