FDA Label for After Bite Xtra
View Indications, Usage & Precautions
After Bite Xtra Product Label
The following document was submitted to the FDA by the labeler of this product Tender Corporation D/b/a Adventure Ready Brands. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredients
Diphenhydramine HCl 2%
Purpose
Topical Analgesic
Uses
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
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 eyes
Stop Use And Ask A Doctor If
conditions worsens if symptoms persist for more than 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children
if swollowed, 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 : consult a doctor
Inactive Ingredients
Aloe Vera, Ciric Acid, Ethyl Alcohol, Glycerin, Methocel, Methylparaben, Oat beta Glucan, Propylparaben, purified water, sodium hydroxide, tea tree oil, vitamin e
Dosage
Adults and children over 2 apply to affected are 3 to 4 times day not more
* Please review the disclaimer below.
