CVS Hemorrhoidal Topical Analgesic description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

CVS Hemorrhoidal Topical Analgesic

CVS PHARMACY, INC.




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                                   Purpose

Dibucaine 1%...................................... Local anesthetic

Purpose

Use

temporarily relives pain and itching due to hemorrhoids or other anorectal disorders

Warnings

For external use only

Allergy Alert

  • Certain persons can develop allergic reactions to ingredietns in this product. If the symptoms being treated does not subside or if redness, irritation, swelling, bleeding or other symptoms develop or increase, discontinue use and ask a doctor.

Do not use

  • in or near the eyes
  • in children under 2 years of age

When using this product

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

Stop use and ask a doctor if

  • bleeding occurs
  • condition worsens or does not improve within 7 days

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 and over: if possible, clean 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 applying
  • apply externally to the affected area up to 3 or 4 times daily
  • children under 12 years of age: ask a doctor

Other information

store at 20-25°C (68-77°F)

Inactive ingredients

disodium EDTA, distilled water, lanolin, mineral oil, white petrolatum

DISTRIBUTED BY:

CVS PHARMACY, INC.

ONE CVS DRIVE

WOONSOCKET, RI 02895 USA

CVS Hemorrhoidal Topical Analgesic

CVS Hemorrhoidal Topical Analgesic

Dibucaine OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-997
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIBUCAINE DIBUCAINE 10 mg

Inactive Ingredients

Ingredient Name Strength
DISODIUM EDTA-COPPER
water
LANOLIN
Mineral Oil
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1 in 1 TUBE
2 NDC:59779-997-28 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2014-01-17


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.