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

do not exceed the recommended daily dosage unless directed by a doctor.

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,

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.

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: ask a doctor.

OTHER INFORMATION

Store below 86° F (30° C).

INACTIVE INGREDIENTS

benzyl alcohol, hydrogenated vegetable oil, tocopheryl acetate

PACKAGE INFORMATION

sunmark®

COMPARE TO TUCKS®
ACTIVE INGREDIENT*
NDC 49348-723-02

hemorrhoidal
suppositories

Relieves hemorrhoidal pain and burning

EASY OPEN STRIPS

12 SUPPOSITORIES

MCKESSON
Empowering Healthcare

Another Quality product Distributed by McKesson
One Post Street, San Francisco, CA 94104
Money Back Guarantee
Please visit us at www.sunmarkbrand.com

*This product is not manufactured or distributed by Pfizer consumer Healthcare, Inc., owner of the registered trademark TUCKS®.

FOR YOUR SAFETY, SUPPOSITORIES ARE PACKAGED IN TAMPER-EVIDENT SEALED PLASTIC WRAPPER.
DO NOT USE IF PLASTIC WRAPPER IS TORN OR OPEN.

HEMORRHOIDAL STARCH
starch suppository

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	49348-723
Route of Administration	RECTAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STARCH, CORN (STARCH, CORN)	STARCH, CORN	0.51 g

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

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	49348-723-02	12 SUPPOSITORY In 1 BOX	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	09/15/2005	06/30/2010

Labeler - McKesson (177667227)

Revised: 02/2010McKesson