MEDICATED WIPES- witch hazel patch 
Meijer Distribution Inc.

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Drug Facts

Active Ingredient

Witch Hazel 50%

Purpose

Hemorrhoidal Astringent

Uses

Temporarily relieves these external symptoms associated with hemorrhoids:

Warnings

For external rectal use only.

When using this product

  • do not exceed the recommended daily dosage unless directed by a doctor.
  • do not insert into rectum or vagina using fingers or mechanical device.

Stop use and ask a doctor if

  • rectal bleeding occurs
  • condition worsens or does not improve within 7 days.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

As hemorrhoidal treatment for adults:

Children under 12 years of age

Other Information

Store at controlled room temperature: 15º-30ºC (59º-86ºF)

Inactive Ingredients

Water, Sodium citrate, Citric acid, Glycerin, Phenoxyethanol, Potassium sorbate

Principal Display Panel

NDC 41250-988-48

meijer

Compare to Preparation H® active ingredient*

medicated wipes

Hemorrhoidal Wipes with Witch Hazel

MAXIMUM STRENGTH

Provides Temporary Relief of Itching, Burning and Irritation

48 WIPES

6 IN x 5 IN (15cm x 12cm)

48

49


NDC 41250-988-96

meijer

Compare to Preparation H® active ingredient*

medicated wipes

Hemorrhoidal Wipes with Witch Hazel

MAXIMUM STRENGTH

Provides Temporary Relief of Itching, Burning and Irritation

For Use with Hemorrhoids and for Vaginal Care

Convenient, Easy to Use

96 WIPES (2 x 48 CT. PACKS)

6 IN x 5 IN (15.2 cm x 12.7 cm)

96

MEDICATED WIPES 
witch hazel patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-988
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg  in 1000 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41250-988-4848 in 1 BOX10/02/2019
1500 mg in 1 PATCH; Type 0: Not a Combination Product
2NDC:41250-988-9696 in 1 BAG10/02/2019
2500 mg in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01506/28/2018
Labeler - Meijer Distribution Inc. (006959555)
Registrant - Meijer Distribution Inc. (006959555)
Establishment
NameAddressID/FEIBusiness Operations
U. S. Nonwovens Corp080453184manufacture(41250-988)

Revised: 1/2024
Document Id: 0ec7062c-6801-a3a8-e063-6394a90aeb78
Set id: ba0f3f9a-95d1-4d8a-86d1-2c25c945118c
Version: 3
Effective Time: 20240112
 
Meijer Distribution Inc.