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

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Medicated Pain Relief

American Sales Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient


Purpose


Use

  • temporarily relieves minor aches and pains of muscles and joints associated with:
    • simple backache
    • arthritis
    • bruises
    • sprains

Warnings

For external use only

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • on a child under 12 years of age with arthritis-like conditions

Ask a doctor before using if you have

  • redness over the affected area

When using this product

  • avoid contact with eyes or mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • excessive skin irritation occurs

Keep out of reach of children.

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

Directions

  • open pouch and remove patch
  • if desired, cut patch to size
  • peel off protective backing and apply sticky side to affected area
  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: consult a doctor

Medicated Pain Relief Other information

  • store at 20 ° to 25 ° C (68 ° F to 77 ° F)


Inactive ingredients

Purified Water, Acrylic Acid, Aluminum Hydroxide, Carboxymethylcellulose sodium, 2-Ethylhexyl Acrylate, Glycerin, Isopropyl Myristate, Methyl Acrylate, Nonoxymol-30, Sodium Polyacrylate, Polyacrylic Acid, Polysorbate 80, Sorbitan Sesquioleate, Starch, Talc, Tartaric acid, Titanium Dioxide

package label

Pain Relieving PatchMedicated Pain Relief

Medicated Pain Relief

Menthol PATCH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-911
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 428.5 mg

Inactive Ingredients

Ingredient Name Strength
water
ACRYLIC ACID
aluminum hydroxide
CARBOXYMETHYLCELLULOSE SODIUM
GLYCERIN
ISOPROPYL MYRISTATE
METHYL ACRYLATE
NONOXYNOL-30
polysorbate 80
SORBITAN SESQUIOLEATE
talc
tartaric acid
titanium dioxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1 in 1 POUCH
2 NDC:41520-911-04 4 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-09-16


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