Drug Facts

Active ingredient

Witch hazel (50% w/w)

Purpose

Astringent

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

For external use only.

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

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

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

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

TUCKS MEDICATED COOLING PADS
witch hazel solution

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	500 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M015	08/30/2016

Labeler - Blistex Inc (005126354)

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