Label: DR BUTLERS HEMORRHOID- witch hazel 50% swab
- NDC Code(s): 70942-100-00, 70942-100-48
- Packager: Beyond Health, PA
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 23, 2025
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- Official Label (Printer Friendly)
- Active Ingredieni
- Purpose
- Uses
- Warnings
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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 up to 6 times daily or after each bowel movement and before applying additional 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.
- Othet Information
- Inactive Ingredients
- 48 count package
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INGREDIENTS AND APPEARANCE
DR BUTLERS HEMORRHOID
witch hazel 50% swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70942-100 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 ROSEMARY (UNII: IJ67X351P9) CHAMOMILE (UNII: FGL3685T2X) LYSINE (UNII: K3Z4F929H6) WATER (UNII: 059QF0KO0R) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) SODIUM CITRATE (UNII: 1Q73Q2JULR) BETAINE (UNII: 3SCV180C9W) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70942-100-48 48 in 1 CONTAINER 07/22/2024 1 NDC:70942-100-00 3 g in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 07/22/2024 Labeler - Beyond Health, PA (026781064)

