Label: MAXIMUM STRENGTH HEMORRHOIDAL PADS- witch hazel cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 49035-465-10, 49035-465-20 - Packager: Walmart, 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 May 10, 2019
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
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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
equateTM
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
equateTM
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
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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 final part346 05/10/2019 Labeler - Walmart, Inc. (051957769)