After Ivy Wipe

Manufacturer
Professional Disposables International, Inc.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:10

Label at a glance#

ProductAfter Ivy Wipe
Active ingredientCAMPHOR (SYNTHETIC)
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor- 3%

OTC - PURPOSE SECTION

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 SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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.

OTC - WHEN USING SECTION

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

OTC - ASK DOCTOR SECTION

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

DOSAGE & ADMINISTRATION SECTION

0.15g Camphor

INACTIVE INGREDIENT SECTION

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

INDICATIONS & USAGE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Web

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10819-880010819-8800-1, 10819-8800-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
47e72184-a6b7-f3de-e063-6394a90a408d47e72751-594d-2887-e063-6294a90a01ae2026-01-08WarningsExact identifier
spl id: 47e72184-a6b7-f3de-e063-6394a90a408d
spl set id: 47e72751-594d-2887-e063-6294a90a01ae

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.