THE ITCH ERASER- diphenhydramine hydrochloride spray 
Adventure Ready Brands

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.

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The Itch Eraser Spray

​Drug Facts

​Active ingredients:

Diphenhydramine HCl 2%

​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

​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

THE ITCH ERASER 
diphenhydramine hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90107-2410
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
OAT (UNII: Z6J799EAJK)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
POVIDONE (UNII: FZ989GH94E)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TEA TREE OIL (UNII: VIF565UC2G)  
ZINC ACETATE (UNII: FM5526K07A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:90107-2410-11 in 1 BOX09/01/2020
128 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/01/2020
Labeler - Adventure Ready Brands (064437304)
Registrant - Adventure Ready Brands (064437304)
Establishment
NameAddressID/FEIBusiness Operations
Adventure Ready Brands064437304manufacture(90107-2410)

Revised: 1/2023
Document Id: f2a1fed2-d2db-5aa9-e053-2a95a90af718
Set id: afd7e738-9cf3-7937-e053-2995a90a55bc
Version: 2
Effective Time: 20230119
 
Adventure Ready Brands