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

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Pramoxine hydrochloride

Libertas Pharma, Inc.

Pramoxine Hydrochloride 1%


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT:

Pramoxine hydrochloride 1%.

INACTIVE INGREDIENTS:

Cetyl alcohol, emulsifying wax, methylparaben, polyoxyethylene C12-C14 ether, PPG5 Ceteth-20, propylene glycol, propylparaben, purified water, sorbitan trioleate, trolamine, and inert propellant: tetrafluoroethane.

INDICATION:

Use for the temporary relief of pain and itching associated with hemorrhoids.

DIRECTIONS: SHAKE WELL BEFORE USE.

Dispense Pramoxine Hydrochloride 1% onto a clean tissue or pad and apply externally to the affected area up to 5 times daily. See carton for additional directions for use.

WARNINGS:

Do not exceed the recommended daily dosage unless directed by a physician. If condition worsens or does not improve within 7 days, consult a physician. In case of rectal bleeding, consult a physician promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator. Certain persons can develop allergic reactions to ingredients in this product. if the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use immediately and consult a physician. Do not use in the eyes or nose. Do not apply to large areas of the body.

CAUTION: FOR EXTERNAL USE ONLY.

Do not insert any part of the aerosol container into the rectum. Contents of the container are under pressure. Do not burn or puncture the aerosol container. Do not store at temperatures above 49°C (120°F).

STORE UPRIGHT AT CONTROLLED ROOM TEMPERATURE 20°-25°C (68°-77°F). DO NOT REFRIGERATE.

Purpose

Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Manufactured for:
Libertas Pharma, Inc.
Lawrenceville, GA 30043

Net Wt. 0.50 oz (15g)

HOLD UPRIGHT TO DISPENSE

PRINCIPAL DISPLAY PANEL

NDC 51862-180-15

For external Use only
HEMORRHOIDAL FOAM-NON STEROID

Pramoxine
Hydrochloride 1%

SHAKE WELL
BEFORE USING

Net Wt. 0.50 oz (15 g)

Libertas
Pharma Inc.

Pramoxine hydrochloride

Pramoxine hydrochloride

Pramoxine hydrochloride AEROSOL, FOAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51862-180
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
pramoxine hydrochloride PRAMOXINE 10 mg

Inactive Ingredients

Ingredient Name Strength
CETYL ALCOHOL
YELLOW WAX
METHYLPARABEN
CETETH-20
propylene glycol
PROPYLPARABEN
water
sorbitan trioleate
TROLAMINE
TETRAFLUOROMETHANE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 CONTAINER
2 NDC:51862-180-15 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2011-10-31


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