PHENYLEPHRINE HYDROCHLORIDE suppository

phenylephrine hydrochloride by

Drug Labeling and Warnings

phenylephrine hydrochloride by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Cocoa butter, 85.5%

Phenylephrine HCI, 0.25%

Shark liver oil, 3.0%

PURPOSE

protectant

vasoconstrictor

protectant

USES

• Temporarily shrinks hemorrhoidal tissue
• Temporarily relieves itching burning and discomfort associated with hemorrhoids
  

WARNINGS

For rectal use only.

Ask a doctor before use if you have

• heart disease
• thyroid disease
• difficulty in urination due to enlargement of the prostate gland
• high blood pressure
• diabetes
  

Ask a doctor or pharmacist before use if you are

presently taking a prescription drug for high blood pressure or depression.

When using this product

do not exceed the recommended daily dosage.

Stop use and ask a doctor if

• you experience bleeding
• condition worsens or does not improve within 7 days.

These may be signs of a serious condition.

If pregnant or breastfeeding

 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 by patting or blotting with an appropriate cleansing tissue. Gently dry by patting or blotting with toilet tissue or soft cloth before insertion of this product.
• Detach one suppository from strip
• Remove wrapper before inserting into rectum
• Hold suppository with rounded end up and insert tip of fingernail at end marked "peel down"
• Carefully peel film slowly and evenly down both sides to expose suppository
• Insert one suppository into rectum up to 4 times daily especially at night and morning or after each bowel movement
  

Children under 12 years:  ask a doctor

SPL UNCLASSIFIED SECTION

STORAGE

Store in a cool place or at room temperature but not over 86° F.

INACTIVE INGREDIENTS

methylparaben, propylparaben, starch

Questions?

Call 1-800-910-6874

BOX INFORMATION - 12 count

up and up

NDC: 11673-394-53

Hemorrohoidal
Suppositories

Compare to Preparation H® Hemorrhoidal Suppositories*

helps shrink swelling of irritated hemrrhoidal tissues
helps relieve itching, burning and discomfort associated with hemorrhoids

12 SUPPOSITORIES

Dist by Tarted Corp. Minneapolis, MN 55403
© Target Brands, Inc.
All rights reserved. Shop Target.com

*This product is not manufactured or distributed by Wyeth Consumer Healthcare, Inc., owner of the registered trademark Preparation H®.

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

INGREDIENTS AND APPEARANCE

PHENYLEPHRINE HYDROCHLORIDE 
phenylephrine hydrochloride suppository

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-394
Route of Administration	RECTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
cocoa butter (UNII: 512OYT1CRR) (cocoa butter - UNII:512OYT1CRR)	cocoa butter	2077 mg
phenylephrine hydrochloride (UNII: 04JA59TNSJ) (phenylephrine - UNII:1WS297W6MV)	phenylephrine hydrochloride	6 mg
shark liver oil (UNII: 4B24275HEU) (shark liver oil - UNII:4B24275HEU)	shark liver oil	73 mg

Inactive Ingredients
Ingredient Name	Strength
methylparaben (UNII: A2I8C7HI9T)
propylparaben (UNII: Z8IX2SC1OH)
starch, corn (UNII: O8232NY3SJ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-394-53	12 in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	09/01/2009

Labeler - Target Corporation (006961700)