After Ivy Wipe

Manufacturer
Tender Corporation d/b/a Adventure Ready Brands | Tender coporation d/b/a Adventure Ready Brands | Professional Disposables International, Inc.
Effective date
2025-11-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:16:35

Label at a glance#

ProductAfter Ivy Wipe
Active ingredientCAMPHOR (SYNTHETIC)
Label structure11 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

WipeWipe

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2700759camphor 3 % Medicated PadPSN3
2700759camphor 30 MG/ML Medicated PadSCD3
2700759camphor 3 % Medicated PadSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix2OH322After Ivy Wipe Art 10.09.2024 FINAL.jpg
Data codeData Matrix5OH32216After Ivy Box Art 10.09.2024 FINAL.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44224-1230-0After Ivy Wipe5 g in 1 POUCHSOLUTION53
44224-1230-1After Ivy Wipe16 in 1 BOXSOLUTION163

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44224-123044224-1230-0, 44224-1230-1

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
After Ivy WipeCAMPHORTender Corporation d/b/a Adventure Ready Brands21d98018-826a-1d0d-e063-6294a90a0a712025-11-17WarningsExact identifier
ndc (package): 44224-1230-1
ndc (package): 44224-1230-0
ndc (product): 44224-1230
ndc11 (package): 44224123000
ndc11 (package): 44224123001
spl id: 43d1d8bf-3afc-8b35-e063-6394a90a875d
spl set id: 21d98018-826a-1d0d-e063-6294a90a0a71

Reported adverse events (FAERS/openFDA)#

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