Medrox description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Medrox

Unit Dose Services
Unit Dose Services

Medrox (Medroxin)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DRUG FACTS:

ACTIVE INGREDIENTS

Methyl Salicylate      20.00%

Menthol                     5.00%

Capsaicin                  0.0375%

PURPOSE

Analgesic/Counterirritant

Analgesic/Counterirritant

External Analgesic

USES

Use for the temporary relief of minor aches and muscle pains associated with arthritis, simple backache, strains, muscle soreness and stiffness.

WARNINGS


  • For external use only. Use only as directed. Avoid contact with eyes and mucous membranes.
  • Do not cover with bandage.
  • Do not use on wounds or damaged skin.

KEEP OUT OF REACH OF CHILDREN

Consult physician for children under 12.


DIRECTIONS


Apply product directly to affected area. Product may be used as necessary, but should not be used more than four times per day.


OTHER INGREDIENTS


Deionized Water, Cetyl Alcohol, PEG-150 Distearate, Isopropyl Myristate, Glycerin, Sodium Lauryl Sulfate, Polysorbate-20, Triethanolamine, Acrylates Copolymer, Propylene Glycol, Methyl Paraben, Propyl Paraben, Diazolidinyl Urea, FD and C Blue 1, D and C Yellow 5

MEDROX (METHYL SALICYLATE, MENTHOL, CAPSAICIN ) OINTMENT

Medrox

Medrox

METHYL SALICYLATE, MENTHOL, CAPSAICIN OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50436-9994(NDC:45861-001)
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
methyl salicylate METHYL SALICYLATE 20 g
MENTHOL 5 g
capsaicin CAPSAICIN 0.0375 g

Inactive Ingredients

Ingredient Name Strength
water
CETYL ALCOHOL
PEG-150 DISTEARATE
ISOPROPYL MYRISTATE
GLYCERIN
SODIUM LAURYL SULFATE
POLYSORBATE 20
TROLAMINE
propylene glycol
METHYLPARABEN
PROPYLPARABEN
DIAZOLIDINYL UREA
FD&C BLUE NO. 1
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50436-9994-1 120 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-02-09


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.