Pre-moistened Hemorrhoidal Pads

Dosage form: solution
Ingredients: witch hazel 0.50mL in 1mL
Labeler: Supervalu Inc
NDC Code: 41163-263

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 INGREDIENT

Witch Hazel 50% v/v

PURPOSE

Hemorrhoidal Astringent

USE For temporary relief of local discomfort, burning, and irritation associated with hemorrhoids

WARNINGS

For external use only. Avoid contact with eyes.

Consult a doctor
  • if condition worsens or does not improve within 7 days
  • in case of bleeding
  • before exceeding the recommended dosage

Do notput this product into rectum using fingers or any mechanical device or applicator






Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS
  • 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 each application of this product. Gently apply to the affected area by patting and then discard. Apply to the affected area up to 6 times daily or after each bowel movement.
  • Children under 12 years of age: consult a doctor.

OTHER INFORMATION

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

OTHER USES For vaginal care - cleanse the area by gently wiping, patting or blotting with pad and discard. Repeat as needed.

INACTIVE INGREDIENTS citric acid, diazolidinyl urea, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate


PACKAGE INFORMATION - 100 COUNT JAR This package is a representation. Packaging is similar for other sizes available.

For your protection, jar is sealed. Remove lid. If seal is broken or missing, do not use.

Equaline

Compare to Tucks® active ingredients*

NDC 41163-263-51

pre-moistened
hemorrhoidal pads
with witch hazel

100 medicated pads


Distributed by
Albertsons, Inc.
Boise, Idaho 83726


*This product is not manufactured or distributed by Parke-Davis, Div. of Warner Lambert Co., owner of the registered trademark TUCKS®.

We're committed to your satisfaction and guarantee the quality of this product. Contact us at 1/877-932-7948, or www.albertsons.com







PACKAGE INFORMATION - 100 COUNT CARTON This package is a representation. Packaging is similar for other sizes available.

For your protection, jar is sealed. Remove lid. If seal is broken or missing, do not use.

Compare to Tucks® active ingredients*

NDC 41163-263-51

pre-moistened
hemorrhoidal pads
with witch hazel

comforts - soothes - cools

uses:

    * to soothe, cool, and comfort itching, burning, and irritation of sensitive rectal areas.
    * an effective hygiene wipe to cleanse rectal area of irritation causing residue
    * provides a fresh and clean feeling
    * solution is pH balanced

100 medicated pads

Distributed by
Albertsons, Inc.
Boise, Idaho 83726


*This product is not manufactured or distributed by Parke-Davis, Div. of Warner Lambert Co., owner of the registered trademark TUCKS®.

We're committed to your satisfaction and guarantee the quality of this product. Contact us at 1/877-932-7948, or www.albertsons.com


PRE-MOISTENED HEMORRHOIDAL PADS 
witch hazel solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-263
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
witch hazel (witch hazel) witch hazel0.50 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
citric acid monohydrate 
diazolidinylurea 
glycerin 
methylparaben 
propylene glycol 
propylparaben 
sodium citrate 
water 
Packaging
#Item CodePackage Description
1NDC:41163-263-5040 APPLICATOR (APPLICATOR) in 1 JAR
12.5 mL in 1 APPLICATOR
2NDC:41163-263-51100 APPLICATOR (APPLICATOR) in 1 JAR
22.5 mL in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34610/01/2004
Labeler - Supervalu Inc (006961411)

Revised: 02/2010
 
Supervalu Inc

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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