Label: GOOD SENSE MEDICATED- witch hazel cloth
- NDC Code(s): 50804-047-60
- Packager: Geiss, Destin & Dunn, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated November 29, 2022
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
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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 discard
- Apply as needed
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For use on children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
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Principal Display Panel
GOOD SENSE
Pre-moistened
N 50804-047-60
Medicated Pads
Hemorrhoidal/Vaginal Pads with Witch Hazel
- Instantly relieves hemorrhoidal burning and itching
- Witch hazel cools, soothes and protects
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®.
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INGREDIENTS AND APPEARANCE
GOOD SENSE MEDICATED
witch hazel clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-047 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 500 mg Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-047-60 100 in 1 JAR; Type 0: Not a Combination Product 12/16/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 12/16/2015 Labeler - Geiss, Destin & Dunn, Inc (076059836)