RELIEF- witch hazel swab

Relief by

Drug Labeling and Warnings

Relief by is a Otc medication manufactured, distributed, or labeled by H and P Industries, Inc. dba Triad Group, H and P Industries, Inc. / Triad Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

SPL UNCLASSIFIED SECTION

STORAGE AND HANDLING

Inactive ingredients

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

QUESTIONS

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

INGREDIENTS AND APPEARANCE

RELIEF 
witch hazel swab

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

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

Inactive Ingredients
Ingredient Name	Strength
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)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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)

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