GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE, WHITE PETROLATUM - glycerin, phenylephrine hydrochloride, pramoxine, white petrolatum cream 
Target Corporation

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.

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DRUG FACTS

ACTIVE INGREDIENTS

Glycerin, USP 14.4%

Phenylephrine HCI, 0.25%

Pramoxine HCI, 1%

White petrolatum, 15%

PURPOSE

Protectant

Vasoconstrictor

Local anesthetic

Protectant

USES

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 product

do 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:
Children under 12 years:  ask a doctor.


OTHER INFORMATION

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

INACTIVE INGREDIENTS

aloe 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 - TUBE

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)

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

tube

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



box

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, TOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.144 mg  in 1 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE0.0025 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE0.01 mg  in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM0.15 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LAURETH-23 (UNII: N72LMW566G)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
PANTHENOL (UNII: WV9CM0O67Z)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-572-241 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: 2/2010
Document Id: dc36f647-2d3c-442b-b16d-7c0ac65414c6
Set id: 0dea93da-f123-4b01-b821-85ea3cd61423
Version: 1
Effective Time: 20100201
 
Target Corporation