GOOD SENSE  MEDICATED- witch hazel cloth 
Geiss, Destin & Dunn, 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

Uses

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

Warnings

For external use only. Avoid contact with eyes.

Stop use and ask a doctor if

  • condition worsens or does not improve within 7 days
  • in case of bleeding

Do Not Use

Do not put 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

Other information

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

Inactive ingredients

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

Principal Display Panel

GOOD SENSE

Pre-moistened

N 50804-047-60

Medicated Pads

Hemorrhoidal/Vaginal Pads with Witch Hazel

Compare to the active ingredient in Tucks®* Medicated Pads*

100% SATISFACTION GURANTEED

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

Label




GOOD SENSE   MEDICATED
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-047
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg
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:50804-047-60100 in 1 JAR; Type 0: Not a Combination Product12/16/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34612/16/2015
Labeler - Geiss, Destin & Dunn, Inc (076059836)

Revised: 11/2022
Document Id: eea13e12-6c7d-3416-e053-2995a90a696b
Set id: 5f122db5-4391-4957-9c25-76834c356c4f
Version: 4
Effective Time: 20221129
 
Geiss, Destin & Dunn, Inc