GOODSENSE MAXIMUM STRENGTH 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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GOODSENSE Maximum Strength Medicated wipes

Active Ingredient

Witch hazel 50%

Purpose

Astringent

Uses

Warnings

For external use only.

When using this product

  • do not exceed the recommended daily dosage unless directed by a doctor
  • do not put this product into 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 a Poison Control Center right away.(1-800-222-1222)

Directions

Other information

Inactive Ingredients

Alcohol, Aloe, citric acid, Decyl Glucoside, Glycerin, Phenoxyethanol, Potassium Sorbate, Propylene Glycol, Sodium Benzoate, Water.

Principal Display Panel

NDC 50804-211-48

GOODSENSE Maximum Strength

Medicated Wipes with Aloe

Hemorrhoidal Wipes with Witch Hazel

Compare to active ingredients of PREPARATION H Medicated Wipes

100% satisfaction Guaranteed

48 Wipes

6 X 5 in. (15.2 X12.7 cm)

Label

GOODSENSE MAXIMUM STRENGTH MEDICATED 
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-211
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL50 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ALOE (UNII: V5VD430YW9)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50804-211-4848 in 1 PACKAGE07/27/2017
12.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34607/27/2017
Labeler - GEISS, DESTIN & DUNN, INC (076059836)
Registrant - GEISS, DESTIN & DUNN, INC (076059836)
Establishment
NameAddressID/FEIBusiness Operations
PREMIER CARE INDUSTRIES, INC858442403manufacture(50804-211)

Revised: 11/2022
Document Id: eea13e12-6c6f-3416-e053-2995a90a696b
Set id: 5453a12b-e775-4101-bd3a-337857e9e167
Version: 4
Effective Time: 20221129
 
GEISS, DESTIN & DUNN, INC