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The Itch Eraser Max Strength

Medically reviewed on December 4, 2017

Dosage form: spray
Ingredients: DIPHENHYDRAMINE HYDROCHLORIDE 20mg in 1mL
Labeler: Tender Corporation
NDC Code: 44224-2410

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.

The Itch Eraser Max Strength Spray

​Drug Facts

​Active ingredients:

Diphenhydramine HCl 2%

​Purpose:

Topical analgesic

​Uses

​For temporary relief of pain and itching associated with:

• insect bites • minor burns • sunburn • minor skin irritations • minor cuts • scrapes • rashes due to poison: ivy, oak and sumac

​Warnings

​For external use only

• do not get into 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.

Do not use

• on large areas of tyhe body • with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

• on chicken pox • on measles

​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

SD Alcohol 40-2, Purified Water, Povidone, Glycerin, Oat Beta Glucan, Sodium Bicarbonate (Baking Soda), Vitamin E Acetate, Tea Tree Oil, and Zinc Acetate

Package Labeling:

THE ITCH ERASER MAX STRENGTH 
diphenhydramine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-2410
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
POVIDONES 
GLYCERIN 
SODIUM BICARBONATE 
.ALPHA.-TOCOPHEROL ACETATE 
TEA TREE OIL 
ZINC ACETATE 
Packaging
#Item CodePackage Description
1NDC:44224-2410-01 BOTTLE, SPRAY in 1 BOX
128 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/04/2015
Labeler - Tender Corporation (064437304)

 
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.

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