Menthol and Zinc Oxide description, usages, side effects, indications, overdosage, supplying and lots more!

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Menthol and Zinc Oxide

Dynarex Corporation
Dynarex Corporation

Calasoothe Ointment


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                         Purpose

Menthol 0.44% v/v                            External Analgesic

                                                          First Aid Antiseptic

                                                          Antipuritic

Zinc Oxide 20.625% v/v                       Skin Protectant

                                                           Moisture Barrier         

Purpose:

A moisture barrier that prevents and helps heal skin irritations from;

  • urine
  • diarrhea
  • perspiration
  • fistula drainage
  • feeding tube site leakage
  • wound drainage (peri-wound skin)
  • minor burns
  • cuts
  • scrapes
  • itching

Warnings:

Keep out of reach of children

  • If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

  • Not for deep or puncture wounds.
  • Avoid contact with eyes.
  • If condition worsens or does not improve within 7 days, consult a doctor

Dosage & Administration:

  • Clean skin with mild skin cleanser
  • Pat dry or allow to air dry
  • Apply a thin layer of Calasoothe to reddened or irritated skin 2-4 times daily, or after each incontinent episode or diaper change to promote comfort and long lasting protection

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

If swallowed , get medical help or contact a Poison Control Center right away.

Inactive Ingredients

Inactive Ingredients: Calamine, Glycerine, Phenol, Lanolin, Heavy Liquid Paraffin, Sodium Bicarbonate, Thymol, White Soft Paraffin

Principal Display Panel

Principal Display Panel - Calasoothe_Ointment

Calasoothe_Ointment.jpg

Menthol and Zinc Oxide

Menthol and Zinc Oxide

Menthol and Zinc Oxide OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67777-234
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL .44 g
Zinc Oxide Zinc oxide 21 g

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
PHENOL
LANOLIN
Mineral Oil
SODIUM BICARBONATE
THYMOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 POUCH
2 71 in 1 JAR
3 113 in 1 TUBE
4 NDC:67777-234-03 24 in 1 CASE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2010-05-11


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Be sure to consult your doctor before taking any medication!
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