Active Ingredients
Diphenhydramine HCl 2%
The following Structured Product Label (SPL) was submitted to the FDA by Tender Corporation D/b/a Adventure Ready Brands for the product After Bite Xtra (NDC 44224-1276). 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.
Diphenhydramine HCl 2%
Topical Analgesic
For the temporary relief of pain and itching associated with minor burns minor cuts oscrapes insect bite minor skin irritations rashes due to poison ivy, poison oak, and poison sumac
For External use only
on large areas of the body with any other product containing diphenhydramine, even one taken by mouth
on chicken pox on measles
avoid contact with eyes
conditions worsens if symptoms persist for more than 7 days or clear up and occur again within a few days
if swollowed, get medical help or contact a poison control center right away.
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 : consult a doctor
Aloe Vera, Ciric Acid, Ethyl Alcohol, Glycerin, Methocel, Methylparaben, Oat beta Glucan, Propylparaben, purified water, sodium hydroxide, tea tree oil, vitamin e
Adults and children over 2 apply to affected are 3 to 4 times day not more
* Please review the disclaimer below.