MEDICATED HEMORRHOIDAL PADS- witch hazel cloth 
Cardinal Health

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

Uses

Warnings

For external use only.

When using this product

  • do not use more than directed unless told to do so by a doctor
  • do not put directly in the rectum by using fingers or any mechanical device or applicator.

Stop use and ask a doctor if

  • bleeding occurs
  • condition worsens or does not improve within 7 days

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away. (1-800-222-1222).

Directions

adults:

children under 12 years of age: consult a doctor

Other Information

Inactive ingredients

Water, Alcohol, Glycerin, Phenoxyethanol, Aloe, Decyl Glucoside, Potassium Sorbate, Propylene Glycol, Sodium Benzoate, Citric Acid.

Questions or Comments?

(800) 320-6603

Principal Display Panel

LEADER TM

NDC 70000-0364-1

Medicated Hemorrhoidal Pads

WITCH HAZEL, 50% | Astringent

Provides Immediate Relief from Itching and Burning Caused by Hemorrhoids

Witch Hazel to Soothe and Protect Irritated Areas

COMPARE TO TUCKS® MEDICATED COOLING PADS active ingredient*

100% Money Back Guarantee

100 PADS

*This product is not manufactured or distributed by McNEIL-PPC, Inc., owner of the registered trademark Tucks® Medicated Cooling Pads.

Label

MEDICATED HEMORRHOIDAL PADS 
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0364
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ALOE (UNII: V5VD430YW9)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70000-0364-11 in 1 CARTON02/13/2019
1100 in 1 JAR
1200 mL in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34602/13/2019
Labeler - Cardinal Health (063997360)

Revised: 11/2022
Document Id: eea0fefa-4a58-2f0f-e053-2a95a90a58b6
Set id: 0b49db40-7abc-4e62-b6da-4b9f5b0ae16d
Version: 6
Effective Time: 20221129
 
Cardinal Health