PREFERRED PLUS HEMORRHOIDAL- phenylephrine hydrochloride, witch hazel cream 
Kinray Inc.

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 ingredients

Phenylephrine hydrochloride 0.25%

Witch hazel 50.0%





For external use only

Ask a doctor before use if you have

  • heart disease
  • high blood pressure
  • diabetes
  • thyroid disease
  • trouble urinating due to an enlarged 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
  • do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

  • bleeding occur
  • condition gets worse 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.


Other information

Inactive ingredients

Principal Display Panel - 1 oz Carton Label

TAMPER-EVIDENT: Do not use if printed "safety sealed" overwrap is broken or missing.

NDC 61715-093-01

Preferred Plus Pharmacy®


Cooling Gel with aloe

*Compare to the active ingredients in PREPARATION H® Cooling Gel

Fast Cooling Relief


Preferred Plus Pharmacy®

NET WT 1 OZ (28 g)

Principal Display Panel - 1 oz Carton Label
phenylephrine hydrochloride, witch hazel cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:61715-093
Route of Administration RECTAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
phenylephrine hydrochloride (UNII: 04JA59TNSJ) (phenylephrine - UNII:1WS297W6MV) phenylephrine hydrochloride 2.5 mg  in 1 L
witch hazel (UNII: 101I4J0U34) (witch hazel - UNII:101I4J0U34) witch hazel 500 mg  in 1 L
Inactive Ingredients
Ingredient Name Strength
aloe vera leaf (UNII: ZY81Z83H0X)  
edetate disodium (UNII: 7FLD91C86K)  
hydroxyethyl cellulose (100 mpa.s at 2%) (UNII: R33S7TK2EP)  
methylparaben (UNII: A2I8C7HI9T)  
polysorbate 80 (UNII: 6OZP39ZG8H)  
propylene glycol (UNII: 6DC9Q167V3)  
propylparaben (UNII: Z8IX2SC1OH)  
water (UNII: 059QF0KO0R)  
sodium citrate (UNII: 1Q73Q2JULR)  
.alpha.-tocopherol acetate (UNII: 9E8X80D2L0)  
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61715-093-01 1 in 1 CARTON
1 0.028 L in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part346 03/28/2014
Labeler - Kinray Inc. (012574513)
Name Address ID/FEI Business Operations
Tropical Products 157469086 MANUFACTURE(61715-093)

Revised: 3/2014
Document Id: beb94d25-40a7-4370-83b4-91bd1db24d11
Set id: 25973c0b-8d76-4736-aca2-9246ed3caf7e
Version: 1
Effective Time: 20140317
Kinray Inc.