MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER- histamine dihydrochloride lotion 
R2 Distribution, LLC

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MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER

MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER



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
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 Product02/07/201702/07/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/27/201402/07/2017
Labeler - R2 Distribution, LLC (967077293)

Revised: 10/2023
 
R2 Distribution, LLC