Medicated Pad description, usages, side effects, indications, overdosage, supplying and lots more!

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Medicated Pad

H and P Industries, Inc. dba Triad Group

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Witch Hazel 50% v/v

PURPOSE

Hemorrhoidal Astringent

USES

For temporary relief of local discomfort, burning, and irritation associated with hemorrhoids

WARNINGS

For external use only. Avoid contact with eyes.

Consult a doctor

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

Do not







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.

OTHER INFORMATION

Store at room temperature: 15°- 30° C (59° - 86° F)

OTHER USES

For vaginal care -

INACTIVE INGREDIENTS

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


LABEL INFORMATION

NDC 50730-7549-1
Compare to the active ingredient in TUCKS®.

Hemorrhoidal
Pads

  • Pre-moistened Hemorrhoidal/Vaginal Pads with Witch Hazel
  • Provides Temporary Relief of Burning, Itching and Local Discomfort Associated with Hemorrhoids


100 MEDICATED PADS

SAFEWAY

For your protection, jar is sealed. Remove lid. If seal is broken or missing, do not use.

DISTRIBUTED BY SAFEWAY INC.
PO BOX 99, PLEASANTON, CA 94566-0009

This product is not manufactured or distributed by Parke-Davis, owner of the registered trademark TUCKS® Medicated Pads.

Medicated Pad

Medicated Pad

witch hazel SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50730-7549
Route of Administration RECTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
WITCH HAZEL .5 mL

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
Diazolidinylurea
GLYCERIN
METHYLPARABEN
propylene glycol
PROPYLPARABEN
SODIUM CITRATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 2.5 in 1 APPLICATOR
2 NDC:50730-7549-1 100 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2007-02-01


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