AFTER IVY WIPE- camphor solution

After Ivy Wipe by

Drug Labeling and Warnings

After Ivy Wipe by is a Otc medication manufactured, distributed, or labeled by Professional Disposables International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Camphor- 3%

PURPOSE

For the temporary relief of pain and itching associated with: insect bites, minor skin irritations, rahses due to poison ivy, poison oak, or sumac.

WARNINGS

When using this product avoid contact with eyes, do not bandage tightly, do not apply to wounds or damaged skin.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a poison control center right away. If in eyes, flush with water for fifteen minutes and calll a doctor.

WHEN USING

Apply to affected area not more than three to four times daily.

ASK DOCTOR

Children under two years do not use, consult a doctor.

DOSAGE & ADMINISTRATION

0.15g Camphor

INACTIVE INGREDIENT

Water, Ethanol, Cocamidopropyl Betaine, Polysorbate 20, Grapefruit Essential Oil, Orange Essential Oil, Lavender Essential Oil

INDICATIONS & USAGE

Temporary relief of pain and itching associated with insect bites, minor skin irritation, rashes due to poinson ivy, poison oak, sumac.

PRINCIPAL DISPLAY PANEL

Web

Box

INGREDIENTS AND APPEARANCE

AFTER IVY WIPE 
camphor solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10819-8800
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	2.295 g  in 76.5 g

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)	0.38 g  in 76.5 g
GRAPEFRUIT OIL (UNII: YR377U58W9)	0.57 g  in 76.5 g
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)	1.5 g  in 76.5 g
WATER (UNII: 059QF0KO0R)	11.48 g  in 76.5 g
ALCOHOL (UNII: 3K9958V90M)	59.67 g  in 76.5 g
BORAGE SEED OIL (UNII: F8XAG1755S)	0.57 g  in 76.5 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10819-8800-2	16 in 1 BOX	01/01/2025
1	NDC: 10819-8800-1	5 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/01/2025

Labeler - Professional Disposables International, Inc. (800777117)