MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER- histamine dihydrochloride lotion

MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER by

Drug Labeling and Warnings

MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER by is a Otc medication manufactured, distributed, or labeled by R2 Distribution, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

MANCORE MUSCLE MEND ROLL-ON PAIN RELIEVER  
histamine dihydrochloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69198-700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	0.6 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69198-700-85	88.7206 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	02/07/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/27/2014

Labeler - R2 Distribution, LLC (967077293)