Label: MEDICATED MULTIPURPOSE WIPES- witch hazel patch
- NDC Code(s): 78691-050-15
- Packager: QUEST USA CORP.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 17, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep Out Of Reach of Children
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Directions
Adults
- unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area.
- use upto 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
- flush or dispose of wipe in trash
- for best results flush no more than one wipe at a time
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Other Information
- store at room temperature 20-25ºC (68-77ºF)
- 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 desired size and place in contact with tissue for a soothing or cooling effect. Leave in place for 15 minutes and repeat as needed.
- Inactive Ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
MEDICATED MULTIPURPOSE WIPES
witch hazel patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78691-050 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 mg in 100 mg Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78691-050-15 15 in 1 BOX 01/17/2024 1 50 mg in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 01/17/2024 Labeler - QUEST USA CORP. (079869689)