Quality Choice Hemorrhoid description, usages, side effects, indications, overdosage, supplying and lots more!

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Quality Choice Hemorrhoid

Chain Drug Marketing Association (CDMA)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Witch Hazel 50%

Purpose

Astringent

Use:

Temporarily relieves these external symptoms associated with hemorrhoids: itching, burning, irritation

Warning

For external use only.

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 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

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 15°-30°C (59°-86°F)

Inactive ingredients:

Water, Glycerin, Alcohol, Propylene Glycol, Sodium Citrate, Diazolidinyl Urea, Citric Acid, Methylparaben, Propylparaben.

Principal Display Panel - Jar Label

NDC 63868-518-01

QC
QUALITY
CHOICE
®

*Compare to the active Ingredient In TUCKS® Medicated Pads

Hemorrhoidal Pads

Medicated Cool Relief

Witch Hazel, 50% - Soothes and Protects

Provides Relief from:

Burning and Itching Caused by Hemorrhoids and Other Rectal and Vaginal Irritations

100 Pads 3.0 in dia (7.62 cm dia)

Quality Choice Hemorrhoid

witch hazel CLOTH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63868-518
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
WITCH HAZEL 500 mg

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
ALCOHOL
propylene glycol
SODIUM CITRATE
DIAZOLIDINYL UREA
CITRIC ACID MONOHYDRATE
METHYLPARABEN
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.001 in 1 CONTAINER
2 NDC:63868-518-01 100 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2014-04-16


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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