Label: GOODSENSE MAXIMUM STRENGTH MEDICATED- witch hazel cloth
- NDC Code(s): 50804-211-48
- 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
- adult: unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area.
- use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discard
- children under 12 years of age:Consult a doctor
- Dispose of wipe in trash.
- do not flush
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Other information
- store at room temperature 20-25°C (68-77°F)
- for vaginal care - cleanse the area by gently wiping, patting, or blotting. Repeat as needed.
- for use as moist compress - if necessary, first cleanse the area as previously described. Fold wipe to desire size and place in contact with tissue for a soothing and cooling effect. Leave in place for 15 minutes and repeat as needed.
- Inactive Ingredients
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Principal Display Panel
NDC 50804-211-48
GOODSENSE Maximum Strength
Medicated Wipes with Aloe
Hemorrhoidal Wipes with Witch Hazel
- Mild everyday wipes
- Cools, Soothes and Cofmorts
- Convenient, Easy to use, Flushable Wipes
Compare to active ingredients of PREPARATION H Medicated Wipes
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48 Wipes
6 X 5 in. (15.2 X12.7 cm)
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INGREDIENTS AND APPEARANCE
GOODSENSE MAXIMUM STRENGTH MEDICATED
witch hazel clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-211 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 50 g in 100 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-211-48 48 in 1 PACKAGE 07/27/2017 1 2.9 g in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 07/27/2017 Labeler - GEISS, DESTIN & DUNN, INC (076059836) Registrant - GEISS, DESTIN & DUNN, INC (076059836) Establishment Name Address ID/FEI Business Operations PREMIER CARE INDUSTRIES, INC 858442403 manufacture(50804-211)