Otc - Active Ingredient
Camphor- 3%
After Ivy Wipe Solution
FDA Label NDC 44224-1230
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tender Corporation D/b/a Adventure Ready Brands for the product After Ivy Wipe (NDC 44224-1230). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, otc - when using, otc - ask doctor, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - 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.
Otc - 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.
Otc - When Using
Apply to affected area not more than three to four times daily.
Otc - 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.
Package Label.Principal Display Panel
* Please review the disclaimer below.
