PAIN RELIEF THERAPY PATCH description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

PAIN RELIEF THERAPY PATCH

UNITED EXCHANGE CORP

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                                                               Purpose

Menthol 5% .....................................................................Topical analgesic

Purpose

Uses temporarily relieves minor pain associated with:

  • arthritis
  • simple backache
  • bursitis
  • tendonitis
  • muscle strains
  • muscle 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 and mucous membranes
  • do not apply to wounds or damaged skin

Stop use 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
  • skin irritation develops

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Directions

adults and children 12 years of age and older:

  • peel off protective backing and apply sticky side to affected area
  • carefully remove backing from patch
  • should be used up to 8 hours
  • should be used no more than 3 times a day

  • consult a doctor

Inactive ingredients: Aloe Barbadensis Leaf Juice, Aluminum Hydroxide, Disodium EDTA, Gelatin, Kaolin, Methylparaben, Glycerin, Titanium Dioxide, Isopropyl Myristate, Purified Water,

Polyvinyl Pyrrolidone, Peg-4 Stearate, Polyvinyl Alcohol, Polysorbate 80, PVP, Tocopherol Acetate, Alumino Magnesium Metasilicate, Castor Oil, Tartaric Acid, BHT, Sodium Polyacrylate.

Distributed by:

UNITED EXCHANGE CORP

17211 Valley View Ave.

Cerritos, CA 90703 USA

MADE IN KOREA

PAIN RELIEF THERAPY PATCH

PAIN RELIEF THERAPY PATCH

MENTHOL PATCH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65923-700
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 750 mg

Inactive Ingredients

Ingredient Name Strength
aluminum hydroxide
EDETATE DISODIUM
GELATIN
KAOLIN
METHYLPARABEN
GLYCERIN
titanium dioxide
ISOPROPYL MYRISTATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65923-700-05 5 in 1 POUCH

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-01-31


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.