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

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Hemorrhoidal Starch

H and P Industries, Inc. dba Triad Group

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Topical starch, 51%

PURPOSE

Protectant

USE

  • Provides temporary relief of the itching, burning and discomfort associated with hemorrhoids and other anorectal disorders
  • Provides a coating to protect irritated tissue

WARNINGS

For rectal use only.

When using this product





Stop use and ask a doctor

  • in case of bleeding
  • if condition worsens or does not improve within 7 days.


If pregnant or breast-feeding,


Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Adults:
  • When practical, cleanse the affected area with mild soap and warm water. Rinse thoroughly.
  • Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product.
  • Detach one suppository from strip of suppositories.
  • Remove film before inserting into the rectum by holding the suppository upright. Carefully separate film by inserting tip of fingernail at film split.
  • Carefully peel film slowly and evenly down both sides to expose suppository
  • Avoid excessive handling of suppository, which is designed to melt at body temperature. If suppository seems soft, hold in film wrapper under cold water for 2 or 3 minutes.
  • Insert one suppository rectally up to 6 times daily or after each bowel movement
Children under 12 years:


OTHER INFORMATION

INACTIVE INGREDIENTS


PACKAGE INFORMATION - REPRESENTATIVE LABEL



HEMORRHOIDAL
SUPPOSITORIES



  • Relieves itching, burning and discomfort
  • Protects and soothes irritated tissue




Hemorrhoidal Starch

Hemorrhoidal Starch

starch SUPPOSITORY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50730-1512
Route of Administration RECTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
STARCH, CORN 0.51 g

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
FAT, HARD
ALPHA-TOCOPHEROL ACETATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50730-1512-1 12 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2006-08-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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