Tucks ® Medicated Cooling Pads - DailyMed

TUCKS MEDICATED COOLING PADS- witch hazel solution  Blistex Inc

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Tucks ® Medicated Cooling Pads

Drug Facts

Active ingredient

Witch hazel (50% w/w)

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 and wash hands

Children under 12 years of age: ask a doctor

Other information

• for use as a moist compress — if necessary, first cleanse the area and place wipe in contact with irritated area for a soothing and cooling effect. Leave in place for up to 15 minutes and repeat as needed but not to exceed directions for use

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 burningand itching caused by hemorrhoids

witch hazel soothes andprotects irritated areas

BRAND USED BY HOSPITALS®

100 PADS

TUCKS MEDICATED COOLING PADS  witch hazel solution

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-2103 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  in 1 mL

Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-2103-2 1 in 1 CARTON 08/30/2016 1 100 in 1 JAR 1 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product 2 NDC:10157-2103-1 1 in 1 CARTON 08/30/2016 2 40 in 1 JAR 2 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product 3 NDC:10157-2103-3 40 in 1 JAR 08/30/2016 3 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product 4 NDC:10157-2103-4 2 in 1 CARTON 08/30/2016 4 100 in 1 JAR 4 1 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 08/30/2016

Labeler - Blistex Inc (005126354)

Establishment
Name	Address	ID/FEI	Business Operations
Blistex Inc	005126354	manufacture(10157-2103)

Revised: 12/2024 Document Id: 7b87eeff-5bf9-4f03-b38a-5d7557ce49bf 34390-5 Set id: b3e68008-3d0d-4124-9579-b503e9fb95c9 Version: 10 Effective Time: 20241213  Blistex Inc