MEDICATED PADS- witch hazel patch

medicated pads by

Drug Labeling and Warnings

medicated pads by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Witch Hazel 50%

Purpose

Hemorrhoidal Astringent

Uses

Temporarily relieves these external symptoms associated with hemorrhoids:

• itching
• burning
• irritation

Warnings

For external use only.

When using this product

• do not exceed the recommended daily dosage unless directed by a doctor.
• do not insert into rectum or vagina using fingers or mechanical device.

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 at 1-800-222-1222.

Directions

As hemorrhoidal treatment for adults:

• when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.
• gently dry by patting or blotting with toilet tissue or soft cloth before applying.
• gently apply to the affected area by patting and then discard.
• can be used up to six times daily or after each bowel movement.

Children under 12 years of age

• consult a doctor.

Other Information

Store at controlled room temperature: 15º-30ºC (59º-86ºF)

Inactive Ingredients

Water, Aloe Barbadensis Leaf Extract, Sodium Citrate, Citric Acid, Glycerin, Phenoxyethanol, Potassium Sorbate

Principal Display Panel

NDC: 11673-614-10

Compare to Tucks®​​*

medicated pads

cooling hemmorhoidal relief

soothing witch hazel helps protect irritated areas

pH balanced

100 PADS

3 IN X 3 IN (7.6 cm X 7.6 cm)

INGREDIENTS AND APPEARANCE

MEDICATED PADS 
witch hazel patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-614
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	50 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-614-10	100 in 1 BOX	05/15/2020
1		50 mg in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	05/15/2020

Labeler - TARGET CORPORATION (006961700)