Tucks Medicated Cooling Pads by Blistex Inc / Accupac LLC

Tucks Medicated Cooling Pads by

Drug Labeling and Warnings

Tucks Medicated Cooling Pads by is a Otc medication manufactured, distributed, or labeled by Blistex Inc, Accupac LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TUCKS MEDICATED COOLING PADS- witch hazel solution 
Blistex LLC

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Active ingredient

Witch hazel (50% w/w)

Purpose

Astringent

Uses

temporarily relieves the local itching and discomfort associated with hemorrhoids

aids in protecting irritated ahorectal areas

temporarily relieves irritation and burning

Warnings

For external use only

Stop use and ask a doctor if

rectal bleeding occurs

condition worsens or does not improve within 7 days

Keep out of the reach of children.

If swallowed, get medical help or call 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 fot the affected area up to 6 times daily or after each bowel movement

Children under 12 years of age: ask a doctor

Other information

DO NOT FLUSH-after application, discard pad in trash and wash hands

for use as a moist compress--if necessary, first cleanse the area and place the wipe in contact with the 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

Water

Glycerin

Sodium Citrate, Unspecified form

Citric Acid Monohydrate

Ethylhexylglycerin

Phenoxyethanol

Edetate Disodium

Potassium Sorbate

label

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
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10157-2103-7	1 in 1 CARTON	08/30/2018	01/15/2026
1		40 in 1 JAR
1		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	08/30/2018	01/15/2026

Labeler - Blistex LLC (005126354)

Registrant - Accupac LLC (071609663)

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

Revised: 1/2026

Document Id: 486e2c85-fc93-2304-e063-6294a90a0ea1

34390-5

Set id: 1f40840d-2566-a77c-e063-6394a90ad494

Version: 2

Effective Time: 20260115