ACTIVE INGREDIENT

Witch Hazel 50%

PURPOSE

Astringent

USES

Temporarily relieves these symptoms associated with hemorrhoids:

itching
burning
irritation

WARNINGS

For external use only.

Stop use and ask a doctor

if condition worsens or does not improve within 7 days
in case of bleeding
before exceeding the recommended dosage

Do not

put this product into rectum 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.

DIRECTIONS

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 each application of this product. Gently apply to the affected area by patting and then discard. Apply to the affected area up to 6 times daily or after each bowel movement.
Children under 12 years of age: consult a doctor.

Inactive ingredients

citric acid, diazolidinyl urea, glycerin, methylparaben, propylene glycol, propylparaben, sodium citrate, water

Package Information

CAT. NO. 10-7540

NDC 50730-7502-1

Relief
Pre-Moistened
Hemorrhoidal Pads
Comforts - Cools - Soothes

Compares to the leading brand

40 PADS

Triad Disposables, Inc.
Brookfield, WI 53045
Made In USA

RELIEF
witch hazel swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50730-7502
Route of Administration	RECTAL, TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
witch hazel (UNII: 101I4J0U34) (witch hazel - UNII:101I4J0U34)	witch hazel	.5 mL

Ingredient Name	Strength
Inactive Ingredients
citric acid monohydrate (UNII: 2968PHW8QP)
diazolidinylurea (UNII: H5RIZ3MPW4)
glycerin (UNII: PDC6A3C0OX)
methylparaben (UNII: A2I8C7HI9T)
propylene glycol (UNII: 6DC9Q167V3)
propylparaben (UNII: Z8IX2SC1OH)
sodium citrate (UNII: 1Q73Q2JULR)
water (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50730-7502-1	40 in 1 JAR

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part346	01/14/1997

Labeler - H and P Industries, Inc. dba Triad Group (050259597)

Registrant - H and P Industries, Inc. dba Triad Group (050259597)

Name	Address	ID/FEI	Business Operations
Establishment
H and P Industries, Inc. / Triad Group		050259597	manufacture

DRUG FACTS