ORAGESIC Oral Pain Reliever description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

ORAGESIC Oral Pain Reliever

Parnell Pharmaceuticals Inc
Parnell Pharmaceuticals Inc

ORAGESIC Oral Pain Reliever


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ORAGESIC Oral Pain Reliever


Active Ingredient

Benzl Alcohol 1%
Menthol 0.04%

Purpose

Oral Pain Reliever

ORAGESIC Oral Pain Reliever Uses

  • temporarily relieves occasional minor irritation, pain, sore mouth and sore throat
  • temporarily relieves pain associated with canker sores.
  • temporarily relieves pain due to minor dental procedures.
  • temporarily relieves pain due to minor irritation of the mouth and gums caused by dentures or orthodontic appliances

Warnings

  • if sore throat is severe, persists for more than 2 days, is accompanied by or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a physician promptly.
  • if sore throat symptoms do not improve in 7 days, or if irritation, pain or redness persists or worsens see your dentist or physician promptly
  • do not exceed recommended dosage

Keep out of reach of children

Enter section text here

Directions

  • use only as directed






Other Information

  • store at room temperature

Inactive Ingredients

ERIODICTYON CALIFORNICUM  (YERBA SANTA), FLAVOR, POLYSORBATE 20, SODIUM CHLORIDE, SORBITOL, WATER

Questions or Comments?

1-800-45-PHARM or 1-800-457-4276

www.parnellpharm.com

U.S. Patent Numbers:

4.938.963; 4.983.378

5.015.474


ORAGESIC Oral Pain Reliever 8oz/237ml (50930-099-08)

ORAGESIC Oral Pain Reliever

ORAGESIC Oral Pain Reliever

BENZYL ALCOHOL, MENTHOL SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50930-099
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZYL ALCOHOL 10 mg
MENTHOL 0.4 mg

Inactive Ingredients

Ingredient Name Strength
ERIODICTYON CALIFORNICUM LEAF
POLYSORBATE 20
SODIUM CHLORIDE
sorbitol
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50930-099-08 237 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2013-01-02


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.