PREFERRED PLUS HEMORRHOID- witch hazel cloth 
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.

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Drug Facts

Active ingredient

Witch Hazel 50%

Purpose

Astringent

Use:

Temporarily relieves these external symptoms associated with hemorrhoids: itching, burning, irritation.

Warning

For external use only.

Using this product: Do not exceed the recommended daily dosage unless directed by a doctor. Do not insert into rectum or vagina using fingers or mechanical device.

Stop use and ask doctor if: Rectal bleeding occurs, condition worsens or does not improve within 7 days.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222

Directions

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before applying. Gently apply to the affected area by patting and then discard. Can be used up to six times daily or after each bowel movement.

Children under 12 years of age: Consult a doctor.

Other Information

Store at controlled room temperature 15°-30°C (59°-86°F)

Inactive ingredients:

Alcohol, Citric Acid, Diazolidinyl Urea, Glycerin, Methylparaben, Propylene Glycol, Propylparaben, Sodium Citrate, Water.

Principal Display Panel - Carton Label

NDC 61715-094-51

Preferred Plus Pharmacy®

*Compare to the active ingredient in TUCKS® Medicated Pads

HEMORRHOIDAL PADS

100 Pads

Maximum Strength Pain Reliever

Principal Display Panel - Carton Label
PREFERRED PLUS HEMORRHOID 
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:61715-094
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
witch hazel (witch hazel) witch hazel500 mg  in 1 L
Inactive Ingredients
Ingredient NameStrength
Water 
Glycerin 
Alcohol 
Propylene Glycol 
Sodium Citrate 
Diazolidinyl Urea 
Citric Acid Monohydrate 
Methylparaben 
Propylparaben 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61715-094-51100 in 1 JAR
10.001 L in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34603/28/2014
Labeler - Kinray, Inc. (012574513)
Establishment
NameAddressID/FEIBusiness Operations
Tropical Products157469086MANUFACTURE(61715-094)

Revised: 3/2014
Document Id: 6f12c3bd-4696-4fb4-9cd9-ac21f8164e91
Set id: cb6a8676-bfad-44d6-aa64-c311ca33966f
Version: 1
Effective Time: 20140318
 
Kinray, Inc.