Medication Guide App

glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum

Dosage form: cream
Ingredients: GLYCERIN 0.144mg in 1g, PHENYLEPHRINE HYDROCHLORIDE 0.0025mg in 1g, PRAMOXINE HYDROCHLORIDE 0.01mg in 1g, PETROLATUM 0.15mg in 1g
Labeler: Target Corporation
NDC Code: 11673-572

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

DRUG FACTS

ACTIVE INGREDIENTSGlycerin, USP 14.4%

Phenylephrine HCI, 0.25%

Pramoxine HCI, 1%

White petrolatum, 15%

PURPOSE

Protectant

Vasoconstrictor

Local anesthetic

Protectant

USES
  • Temporarily relieves pain, soreness and burning
  • Helps relieve the local itching and discomfort associated with hemorrhoids
  • Temporarily shrinks hemorrhoidal tissue
  • Temporarily provides a coating for relief of anorectal discomforts
  • Temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

WARNINGS


Ask a doctor before use if you have
  • heart disease
  • thyroid disease
  • high blood pressure
  • diabetes
  • difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

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

When using this productdo not exceed the recommended daily dosage unless directed by a doctor

Stop use and ask a doctor if
  • bleeding occurs
  • the introduction of the applicator causes additional pain
  • condition worsens or does not improve within 7 days
  • an allergic reaction develops
  • the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase


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 wipe. Gently dry by patting or blotting with a tissue or soft cloth before applying cream.
  • When first opening the tube, puncture foil seal with top end of cap
  • Apply externally or in the lower portion of the anal canal only
  • Apply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement
  • For application in the lower anal canal: remove cover from dispensing cap. Attach dispensing cap to tube. Lubricate applicator well, then gently insert applicator into the rectum.
  • Thoroughly clean dispensing cap after each use and replace cover
Children under 12 years:  ask a doctor.


OTHER INFORMATIONStore at room temperature: 20° - 25° C (68° - 77° F)

INACTIVE INGREDIENTSaloe barbadensis leaf extract, BHA, carboxymethylcellulose sodium, cetyl alcohol, citric acid, edetate disodium, glyceryl stearate, laureth-23, methylparaben, mineral oil, panthenol, propyl gallate, propylene glycol, propylparaben, purified water, sodium benzoate, steareth-2, steareth-20, stearyl alcohol, tocopherol. vitamin E, xanthan gum

Questions?

Call 1-800-910-6874

PACKAGE INFORMATION - TUBEup and up

NDC 11673-572-24

Hemorrhoidal Cream

maximum strength

Compare to Preparation H® Hemorrhoidal Cream*

Helps shrink swelling of irritated hemorrhoidal tissues

NET WT 1.8 OZ (51 g)

This tube is sealed and packaged in a carton. Do not buy if carton is missing . Do not use if the seal under the cap has been punctured or if the tube is damaged.

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

Dist. by Target Corp.
Minneapolis, MN 55403
Made in U.S.A.

® and © 2009 Target Brands, Inc.
All Rights Reserved
Shop Target.com


PACKAGE INFORMATION - BOX

up and up

NDC 11673-572-24

Hemorrhoidal Cream

maximum strength

Compare to Preparation H® Hemorrhoidal Cream*

Helps shrink swelling of irritated hemorrhoidal tissues

NET WT 1.8 OZ (51 g)

DO NOT USE IF SEAL UNDER CAP OF TUBE IS BROKEN OR MISSING WHEN PURCHASED.

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

Distributed by Target Corporation
Minneapolis, MN 55403
Made in U.S.A.

® and © 2009 Target Brands, Inc.
All Rights Reserved
Shop Target.com



GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE, WHITE PETROLATUM 
glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-572
Route of AdministrationRECTAL, TOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN0.144 mg  in 1 g
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE0.0025 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE0.01 mg  in 1 g
PETROLATUM (PETROLATUM) PETROLATUM0.15 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
BUTYLATED HYDROXYANISOLE 
CARBOXYMETHYLCELLULOSE SODIUM 
CETYL ALCOHOL 
ANHYDROUS CITRIC ACID 
EDETATE DISODIUM 
GLYCERYL MONOSTEARATE 
LAURETH-23 
METHYLPARABEN 
LIGHT MINERAL OIL 
PANTHENOL 
PROPYL GALLATE 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
SODIUM BENZOATE 
STEARYL ALCOHOL 
ALPHA-TOCOPHEROL 
.ALPHA.-TOCOPHEROL ACETATE, DL- 
XANTHAN GUM 
Packaging
#Item CodePackage Description
1NDC:11673-572-241 TUBE, WITH APPLICATOR (TUBE) in 1 BOX
151 g in 1 TUBE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34604/01/2009
Labeler - Target Corporation (006961700)

Revised: 02/2010
 
Target Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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