TUCKS MEDICATED COOLING PADS- witch hazel solution 
Blistex 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% w/w)

Purpose

Astringent

Uses

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:

Children under 12 years of age: ask a doctor

Other information

Inactive ingredients

citric acid, disodium EDTA, ethylhexylglycerin, glycerin, phenoxyethanol, potassium sorbate, purified water, sodium citrate

PRINCIPAL DISPLAY PANEL - 100 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

BRAND USED BY HOSPITALS®

100 PADS

PRINCIPAL DISPLAY PANEL - 100 Pad Jar Carton
TUCKS MEDICATED COOLING PADS 
witch hazel solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10157-2103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL500 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10157-2103-21 in 1 CARTON08/30/2016
1100 in 1 JAR
11 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2NDC:10157-2103-11 in 1 CARTON08/30/2016
240 in 1 JAR
21 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3NDC:10157-2103-340 in 1 JAR08/30/2016
31 mL in 1 APPLICATOR; Type 0: Not a Combination Product
4NDC:10157-2103-42 in 1 CARTON08/30/2016
4100 in 1 JAR
41 mL in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34608/30/2016
Labeler - Blistex Inc (005126354)
Establishment
NameAddressID/FEIBusiness Operations
Blistex Inc005126354manufacture(10157-2103)

Revised: 12/2021
Document Id: a6a8c255-ec4c-412b-8243-bccc63b231b2
Set id: b3e68008-3d0d-4124-9579-b503e9fb95c9
Version: 9
Effective Time: 20211215
 
Blistex Inc