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 Type HUMAN OTC DRUG Item Code (Source) NDC:61715-094
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
witch hazel (UNII: 101I4J0U34) (witch hazel - UNII:101I4J0U34) witch hazel 500 mg  in 1 L
Inactive Ingredients
Ingredient Name Strength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Alcohol (UNII: 3K9958V90M)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sodium Citrate (UNII: 1Q73Q2JULR)  
Diazolidinyl Urea (UNII: H5RIZ3MPW4)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61715-094-51 100 in 1 JAR
1 0.001 L in 1 CONTAINER
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)
Establishment
Name Address ID/FEI Business Operations
Tropical Products 157469086 MANUFACTURE(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.