MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER (HISTAMINE DIHYDROCHLORIDE) LOTION [R2 DISTRIBUTION, LLC]

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MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER (HISTAMINE DIHYDROCHLORIDE) LOTION [R2 DISTRIBUTION, LLC]
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NDC 69198-700-85
Set ID 666fe6d8-8176-4005-8fde-30fca1ec9613
Category HUMAN OTC DRUG LABEL
Packager R2 Distribution, LLC
Generic Name
Product Class
Product Number
Application Number PART348
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  • MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER


  • ACTIVE INGREDIENT


    Active Ingredient / Purpose

    Histamine DHCl 0.06% / External Analgesic

  • Uses

    For temporary relief of minor aches and pains of muscles and joints associated with arthritis, backache and sprains

  • Warnings

    Use only as directed. For external use only. Not intended for persons under the age 18.

    When using this product:

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

    Stop use and ask a doctor if:

    • symptoms persist for more than seven days
    • you experience irritation, redness or discomfort
  • Directions:

    Apply directly to effected area. Do not use more than four times per day.

  • Other information:

    Do not use if tamper resistant seal is broken. Store in a cool, dry place and avoid excessive heat or cold.

    Keep out of reach of children.

  • Inactive Ingredients:

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cetearyl Olivate, Cocos Nucifera (Coconut) Oil, Eucalyptus Globulus Oil, Gluconolactone, Glycerin, Methylsulfonylmethane (MSM), Salix Alba (Willow Bark) Extract, Sodium Benzoate, Sodium Hydroxide, Sorbitan Olivate, Xanthan Gum, Zemea (Corn) Propanediol

  • MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER 3OZ (69198-700-85)

    MuscleMend
  • INGREDIENTS AND APPEARANCE
    MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER  
    histamine dihydrochloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69198-700
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE0.6 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    WILLOW BARK (UNII: S883J9JDYX)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69198-700-8588.7206 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product02/07/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34808/27/2014
    Labeler - R2 Distribution, LLC (967077293)
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