PREPARATION H TOTABLES IRRITATION RELIEF WIPES- witch hazel cloth 
Haleon US Holdings LLC

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Drug Facts

Active ingredient

Witch hazel 50.0%

Purpose

Astringent

Uses

Warnings

For external use only

When using this product

  • do not exceed the recommended daily dosage unless directed by a doctor
  • do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

  • 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.

Directions

Other information

Inactive ingredients

aloe barbadensis leaf juice, anhydrous citric acid, capryl/capramidopropyl betaine, diazolidinyl urea, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate

Questions or comments?

Call weekdays 9 AM to 5 PM EST at 1-800-99PrepHor 1-800-997-7374.

For most recent product information, visit www.preparationh.com.

PRINCIPAL DISPLAY PANEL

PREPARATION H ®

MEDICATED
HEMORRHOIDAL
WIPES

WITH WITCH HAZEL

MAXIMUM STRENGTH FORMULA

WITH
ALOE

Tōtables ®

Irritation Relief

10 INDIVIDUALLY WRAPPED FLUSHABLE WIPES
5.375 x 6.25 in. (13.6 x 15.8 cm)

Principal Display Panel - 10 Wipe Packet Carton
PREPARATION H TOTABLES IRRITATION RELIEF WIPES 
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0573-0558
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL5 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CAPRYL/CAPRAMIDOPROPYL BETAINE (UNII: 231H3ZT9NE)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0573-0558-0710 in 1 CARTON11/21/2010
11 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01511/21/2010
Labeler - Haleon US Holdings LLC (079944263)

Revised: 2/2024
Document Id: 128b4b14-27ae-e6ea-e063-6394a90a8f3a
Set id: 1953ec64-20ce-488b-8f14-44e15cc9e720
Version: 5
Effective Time: 20240229
 
Haleon US Holdings LLC