Ivy-Dry Super description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Ivy-Dry Super

Ivy-Dry, Inc.

Ivy-Dry Super


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Benzyl Alcohol 10%

Camphor 0.5%

Menthol 0.25%

Purpose

External Analgesic

Ivy-Dry Super Uses


  • for the temporary relief of itching associated with insect bites and minor skin irritations

For external use only.

Do not use

  • on face or genital areas
  • on areas of blistered or broken skin
  • with a compress after application

When using this product

  • do not get into eyes
  • if contact occurs, flush eyes with water

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days.

If pregnant or breast-feeding,

ask a doctor before use.

Keep out of reach of children.

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

Directions


  • Apply to affected area not more than 3 times daily.
  • Children under 6 years of age: do not use, ask a doctor.
  • Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary.
  • Test product on small patch of skin before applying to the entire body.

Ivy-Dry Super Other information

Store at room temperature

You may report a serious adverse reaction to Report Reaction, LLC PO Box 22 Plainsboro, NJ 08536-0222

Inactive Information

Water, Isopropanol, Zinc Acetate, Isoceteth-20, Zinc Lactate.

Package Labeling



Ivy-Dry Super

Continuous Spray

TEMPORARY RELIEF OF PAIN AND ITCHING

External Analgesic

Manufactured for:
Ivy-Dry, Inc.
299-B Fairfield Avenue
Fairfield, NJ 07070
Made In Canada
©2012 Ivy-Dry, Inc.
Questions or Comments
www.ivydry.com



Ivy-Dry Super

Ivy-Dry Super

BENZYL ALCOHOL, CAMPHOR, MENTHOL SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49546-105
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZYL ALCOHOL 10 mL
CAMPHOR (SYNTHETIC) 0.5 mL
MENTHOL 0.25 mL

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL ALCOHOL
ZINC ACETATE
isoceteth-20
zinc lactate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49546-105-03 89 in 1 CANISTER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-07-11


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.