Label: FLUSHABLE HEMORRHOIDAL MEDICATED WIPES MAXIMUM STRENGTH- witch hazel cloth
- NDC Code(s): 72288-923-01, 72288-923-02
- Packager: Amazon.com Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 24, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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
- 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 topical hemorrhoidal treatments, and then discard
- children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
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PRINCIPAL DISPLAY PANEL
Amazon Basics
Flushable Hemorrhoidal Medicated Wipes
Maximum Strength
Compare to the active ingredient of Preparation H(R) Medicated Wipes*
- Temporary Relief of irritation and burning
- Convenient, easy to use
- Flushable and Safe for Well-maintained sewer and septic Systems**
Active Ingredient: Witch Hazel 50%
2x48 COUNT | 5IN x 6 IN (12CM x 15.2CM)
4x48 COUNT | 5IN x 6 IN (12CM x 15.2CM)
Made in USA from domestic and imported materials
*this product is not manufactured or distributed by Haleon US Holdings, LLC owner of the registered trademark Preparation H
Distributed by Amazon.com services LLC, Seattle WA 98109
1-877-485-0385
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INGREDIENTS AND APPEARANCE
FLUSHABLE HEMORRHOIDAL MEDICATED WIPES MAXIMUM STRENGTH
witch hazel clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72288-923 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 0.5 g Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CITRATE (UNII: 1Q73Q2JULR) BRONOPOL (UNII: 6PU1E16C9W) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) PEG-75 LANOLIN (UNII: 09179OX7TB) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72288-923-02 2 in 1 CARTON 01/01/2026 1 NDC:72288-923-01 48 in 1 CELLO PACK; Type 0: Not a Combination Product 2 NDC:72288-923-01 48 in 1 CELLO PACK; Type 0: Not a Combination Product 01/01/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 01/01/2026 Labeler - Amazon.com Services LLC (128990418)