TUCKS MEDICATED COOLING PADS- witch hazel cloth 
Johnson & Johnson Consumer Inc.

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.

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Tucks Medicated Cooling Pads

Drug Facts

Active ingredient

Witch hazel 50%

Purpose

Astringent

Uses

  • temporarily relieves the local itching and discomfort associated with hemorrhoids
  • aids in protecting irritated anorectal areas
  • temporarily relieves irritation and burning

Warnings

For external use only.

When using this product

  • do not use more than directed unless told to do so by a doctor
  • do not put directly in the rectum by using fingers or any mechanical device or applicator

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.

Directions

Adults

  • when practical, clean the affected area with mild soap and warm water, and rinse thoroughly
  • gently dry by patting or blotting with toilet tissue or a soft cloth before applying
  • apply externally to the affected area up to 6 times daily or after each bowel movement
  • after application, discard pad

Children under 12 years of age: ask a doctor.

Other information

store at 68°-77°F (20° -25°C)

Inactive ingredients

water, glycerin, propylene glycol, sodium citrate, citric acid, diazolidinyl urea, methylparaben, propylparaben

Questions?

800-223-0182; Outside US, dial collect 215-273-8755

Distributed by: McNEIL-PPC, Inc.
Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 40 Pad Jar Carton

TUCKS®

MEDICATED COOLING PADS

HEMORRHOIDAL PADS WITH WITCH HAZEL

immediate relief from burning
and itching caused by hemorrhoids

witch hazel soothes and
protects irritated areas

40 PADS

Principal Display Panel - 40 Pad Jar Carton
TUCKS MEDICATED COOLING PADS 
witch hazel cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30014-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Witch Hazel (UNII: 101I4J0U34) (Witch Hazel - UNII:101I4J0U34) Witch Hazel500 mg
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
Diazolidinyl Urea (UNII: H5RIZ3MPW4)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:30014-102-401 in 1 CARTON07/01/200705/01/2018
140 in 1 JAR; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
2NDC:30014-102-991 in 1 CARTON07/01/200705/01/2018
2100 in 1 JAR; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
3NDC:30014-102-942 in 1 PACKAGE, COMBINATION07/01/200705/01/2018
31 in 1 CARTON
3100 in 1 JAR; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34607/01/200705/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 10/2016
Document Id: dde28243-e8e2-4326-9663-70964271974b
Set id: 81f2d66b-7ec6-42ea-acef-b93872eb0cac
Version: 4
Effective Time: 20161005
 
Johnson & Johnson Consumer Inc.