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AfterBite with Antihistimine

Dosage form: cream
Labeler: Tender Corporation
NDC Code: 44224-0007

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

AfterBite with Antihistimine

Active Ingredient

Diphenhydramine 2%


Topical Analgesic


For temporary relief of pain and itching caused by

  • insect bites
  • minor burns
  • minor skin irritation
  • minor cuts and scrapes


For external use only.

When using this product
  • do not get into eyes

Do not use

on chicken pox, poison ivy, sunburn, large areas of the body, broken, blistered or oozing skin, more often than directed, or with any other product containing diphenhydramine, even one taken by mouth.

Stop use and ask a doctor if
  • condition worsens
  • symptoms persist for 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. If in eyes flush with water for 15 minutes and call a doctor

  • Do not use more than directed
  • Adults and children 2 years and older apply to the affected area not more than 3 to 4 times daily
  • Children under 2 years ask a doctor
  • For a bee sting, remove stinger before treatment

Inactive Ingredients

Ammonia, Carbomer, Glycerin, Purified Water, and Tea Tree Oil

The Itch Eraser

Trusted After Bite now in a PLUS formula - with Antihistamine! Quickly stops the pain, itching and discomfort of insect bites and stings!

SATISFACTION GUARANTEED: Return product to place of purchase or manufacturer.

Tender Corporation
Littleton, NH 03561
Made in USA

See our complete line of products for the treatment and prevention of outdoor ailments at

Product Labeling

AfterBite The Itch Eraser
with Antihistimine

Instant Pain Relief

stop the Itching and Discomfort

BE READY for Mosquitoes

Black Flies
Bees and Wasps
Ticks and
other Skin Irritations

diphenhydramine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-0007
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:44224-0007-11 TUBE (TUBE) in 1 BOX
120 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/03/2012
Labeler - Tender Corporation (064437304)

Revised: 07/2012
Tender Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.