Marathon Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Marathon Pain Relief

Cosmetic Specialty labs, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Menthol 3.0%

PURPOSE

Topical analgesic

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a poison control center right away.

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
  • do not bandage tightly or use with heating pad
  • avoid contact with eyes or mucus membranes
  • do not apply to wounds or damaged skin

Stop using 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 deveops

If pregnant or breast-feeding

ask a health professional before use

DIRECTIONS

adults and children over 12 years

  • apply generously to affected area
  • massage into painful area until throughly absorbed into skin
  • repeat as necessary, but no more than 4 times daily

children 12 years or younger

ask a doctor

INACTIVE INGREDIENTS

Aloe Barbadensis Leaf, Anthemis Nobilis Extract, Arnica Montana Flower Extract, Blue 1, Butylene Glycol, Calendula Officinalis Extract, Capsicum rutescens Fruit, Carbomer, Centaurea Cyanus Extract, Cetearyl Alcohol, Coriandrum Sativum (Coriander) Fruit Oil, Emu Oil, Fragrance, Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Hypericum Perforatum Extract, Matricaria Chamomilla Extract, Methylsulfonylmethane, Purified Water, Salix Alba (Willow) Baril Extract, SD Alcohol 40, Sorbitol, Tetrasodium EDTA, Tilia Sylvestris Extract, Triethanolamine.

PRINCIPAL DISPLAY PANEL

Marathon Pain Relief

Marathon Pain Relief

Menthol 3.0% LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58133-001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 3 g

Inactive Ingredients

Ingredient Name Strength
Aloe Vera Leaf
CHAMAEMELUM NOBILE FLOWER
ARNICA MONTANA FLOWER
FD&C BLUE NO. 1
BUTYLENE GLYCOL
CALENDULA OFFICINALIS FLOWER
Capsicum
CARBOMER 934
Centaurea Cyanus Flower
CETOSTEARYL ALCOHOL
CORIANDER OIL
EMU OIL
HAMAMELIS VIRGINIANA TOP
Hypericum Perforatum
CHAMOMILE
DIMETHYL SULFONE
water
SALIX ALBA BARK
ISOPROPYL ALCOHOL
sorbitol
EDETATE SODIUM
TILIA X EUROPAEA FLOWER
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58133-001-13 113 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-03-15


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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