IVY-DRY SUPER- benzyl alcohol, camphor, menthol spray

Ivy-Dry Super by

Drug Labeling and Warnings

Ivy-Dry Super by is a Otc medication manufactured, distributed, or labeled by Ivy-Dry, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzyl Alcohol 10%

Camphor 0.5%

Menthol 0.25%

Purpose

External Analgesic

Uses

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

WARNINGS

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.

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

Sprays at any angle!

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

INGREDIENTS AND APPEARANCE

IVY-DRY SUPER 
benzyl alcohol, camphor, menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49546-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH)	BENZYL ALCOHOL	100 mg  in 1 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	5 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ZINC ACETATE (UNII: FM5526K07A)
ISOCETETH-20 (UNII: O020065R7Z)
ZINC LACTATE (UNII: 2GXR25858Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49546-105-03	89 mL in 1 CANISTER; Type 0: Not a Combination Product	07/11/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/11/2012

Labeler - Ivy-Dry, Inc. (800544590)