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Tucks

Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

Tucks Fast Relief Spray


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Pramoxine HCL 1%

Purpose

Pain reliever

Use

  • temporary relieves these local symptoms associated with hemorrhoids:
    • pain
    • itching
    • discomfort

Warnings

For external use only

When using this product

  • do not use more than directed unless told to do so by a doctor
  • do not put into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

  • allergic reaction occurs
  • redness, irritation, swelling, pain, or other symptoms begin or increase
  • rectal bleeding occurs
  • condition worsens or does not improve within 7 days

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

Directions

  • adults and children 12 years of age and older: apply to the affected area up to 5 times daily
    • when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly
    • gently dry by patting or blotting with toilet tissue or a soft cloth before application
  • children under 12 years of age: ask a doctor

Tucks Other information

  • store at 20 to 25°C (68-77°F)

Inactive ingredients

aloe barbadensis leaf juice, denatonium benzoate, ethyl alcohol, polysorbate 20, t-butyl alcohol, tocopheryl acetate, water

Questions?

call toll-free 800-223-0182 or 215-273-8755 (collect)

Distributed by: Johnson & Johnson
Healthcare Products
Division of McNEIL-PPC, Inc.
Skillman, NJ 08558-9418
©McNEIL-PPC, Inc. 2012

PRINCIPAL DISPLAY PANEL - 14.8 mL Bottle Label

NEW

USE AT HOME OR
ON=THE-GO

TUCKS®

FAST RELIEF SPRAY

HEMORRHOIDAL SPRAY

Relieves pain,
itching and burning

clean feeling spray

sprays
upside-down

BRAND USED
BY HOSPITALS

0.5 fl oz (14.8mL)

Tucks

Tucks

Pramoxine Hydrochloride SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-504
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
Aloe Vera Leaf
denatonium benzoate
ALCOHOL
POLYSORBATE 20
ALPHA-TOCOPHEROL ACETATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 14.8 in 1 BOTTLE, SPRAY
2 NDC:42002-504-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2012-04-17


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Be sure to consult your doctor before taking any medication!
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