Label: MAXIMUM STRENGTH HEMORRHOIDAL PADS- witch hazel cloth
- NDC Code(s): 49035-465-10, 49035-465-20
- Packager: Walmart, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 14, 2025
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
As hemorrhoidal treatment for adults:
- when practial 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 applying.
- gently apply to the affected area by patting and then discard
- can be used up to six times daily or after each bowel movement
children under 12 years of age:consult a doctor
- Other information
- Inactive ingredients
- Questions or Comments?
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Principal Display Panel
NDC 49035-465-10
equate TM
Maximum Strength Hemorrhoidal Pads
Compare to the active ingredient in TUCKS ®Medicated Pads*
Medicated cool relief with witch hazel soothes and provides temporary relief of hemorrhoidal irritation and burning
- For use with hemorrhoids and vaginal care
- Protects irritated areas
- Convenient and easy to use
100 PADS
NDC 49035-465-20
equate TM
Maximum Strength Hemorrhoidal Pads
Compare to the active ingredient in TUCKS® Medicated Pads*
Medicated cool relief with witch hazel soothes and provides temporary relief of hemorrhoidal irritation and burning
- For use with hemorrhoids and vaginal care
- Protects irritated areas
- Convenient and easy to use
200 PADS
-
INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH HEMORRHOIDAL PADS
witch hazel clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-465 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) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-465-10 100 in 1 JAR; Type 0: Not a Combination Product 05/10/2019 2 NDC:49035-465-20 200 in 1 JAR; Type 0: Not a Combination Product 05/10/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 05/10/2019 Labeler - Walmart, Inc. (051957769)