Label: REAL TIME PAIN RELIEF MAXX PLUS TOPICAL ANALGESIC- menthol lotion

  • NDC Code(s): 84573-547-03, 84573-547-04, 84573-547-05, 84573-547-07, view more
    84573-547-12, 84573-547-16
  • Packager: Real Time Products Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 12, 2024

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  • Drug Facts

  • Active Ingredient

    Menthol 1.9%

    Purpose

    Topical Analgesic

  • Uses:

    Temporarily relieves minor pain associated with: Arthritis

    • Simple Backache 
    • Muscle Strains
    • Sprains
    • Bruises
    • Cramps
  • Warnings:

    For external use only

    When using this product:

    Use only as directed

    • Avoid contact with eyes or mucous membranes
    • Do not apply to wounds or damaged skin
    • Do not bandage tightly

    Stop use and ask a doctor if:

    Condition worsens

    • Symptoms persist for more than 7 days or clear up and occur again within a few days 
    • Redness is present
    • Irritation develops

    Keep out of reach of children.

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

  • Directions:

    Adults and Children over 2 years: Apply to affected area. Massage into painful area until thoroughly absorbed into skin. Repeat as necessary, but no more than 4 times daily. Children 2 years or younger: ask a doctor.

  • Other Ingredients:

    *Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Cannabis Sativa (Hemp)Seed Oil, Caprylyl Glycol, Capsaicin, Centaurea Cyanus (Cornflower) Extract, Chamomilla Matricaria (Chamomile) Extract, Chondroitin Sulfate, Coriandrum Sativum (Coriander) Fruit Oil, Emu Oil, Glucosamine Sulfate, Glycerin, Hamamelis Virginiana (Witch Hazel), Hypericum Perforatum (St. John's Wort) Extract, C13-14 Isoparaffin, Laureth-7, Mentha Piperita (Peppermint) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Salix Alba (Willow) Bark Extract, SD-Alcohol 40B, Sorbitol, Tilia Cordata (Linden) Bark Extract. *Denotes certified organic ingredient.

  • Questions?

    877-787-7180

  • Package Labelling: 88ml

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  • Package Labelling: 120ml

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  • Package Labelling: 147.8ml

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  • Package Labelling: 210ml

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  • Package Labelling: 354ml

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  • Package Labelling: 473ml

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  • INGREDIENTS AND APPEARANCE
    REAL TIME PAIN RELIEF MAXX PLUS TOPICAL ANALGESIC 
    menthol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84573-547
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL19 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    HEMP (UNII: TD1MUT01Q7)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CAPSAICIN (UNII: S07O44R1ZM)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CORIANDER OIL (UNII: 7626GC95E5)  
    EMU OIL (UNII: 344821WD61)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    ST. JOHN'S WORT (UNII: UFH8805FKA)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    LAURETH-7 (UNII: Z95S6G8201)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SALIX ALBA (WILLOW) BARK EXTRACT (UNII: 205MXS71H7)  
    SORBITOL (UNII: 506T60A25R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84573-547-0388 mL in 1 TUBE; Type 0: Not a Combination Product10/23/2024
    2NDC:84573-547-04120 mL in 1 TUBE; Type 0: Not a Combination Product10/23/2024
    3NDC:84573-547-05147.8 mL in 1 TUBE; Type 0: Not a Combination Product10/23/2024
    4NDC:84573-547-07210 mL in 1 TUBE; Type 0: Not a Combination Product10/23/2024
    5NDC:84573-547-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product10/23/2024
    6NDC:84573-547-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/23/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/23/2024
    Labeler - Real Time Products Inc. (117624292)
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