Active Ingredients:
Diphenhydramine HCl 2%
The Itch Eraser
FDA Label NDC 90107-2410
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Adventure Ready Brands for the product The Itch Eraser (NDC 90107-2410). 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 active ingredients:, purpose:, uses, warnings, do not use, ask a doctor before use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose:
Topical analgesic
Uses
For temporary relief of pain and itching associated with:
• minor burns
• sunburn
• minor cuts
• insect bites
• minor skin irritations
• rashes due to poison ivy, poison oak, and poison sumac
Warnings
For external use only
Do Not Use
• on large areas of the body
• with any other product containing diphenhydramine, even one taken by mouth
Ask A Doctor Before Use
• on chicken pox • on measles
When Using This Product
avoid contact with the eyes.
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
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- do not use more often than directed
- adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.
- children under 2 years of age: ask a doctor.
Inactive Ingredients
Glycerin, Oat Beta Glucan, Povidone, Purified Water, SD Alcohol 40-2, Sodium Bicarbonate (Baking Soda), Tea Tree Oil, Vitamin E Acetate, Zinc Acetate
Package Labeling
Box (0002 1261 2 Itcheraser Spray Box)
* Please review the disclaimer below.
