THE ITCH ERASER- diphenhydramine hydrochloride spray

The Itch Eraser by

Drug Labeling and Warnings

The Itch Eraser by is a Otc medication manufactured, distributed, or labeled by Adventure Ready Brands. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​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

• ​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

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

INGREDIENTS AND APPEARANCE

THE ITCH ERASER 
diphenhydramine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90107-2410
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90107-2410-1	1 in 1 BOX	09/01/2020
1		28 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/01/2020

Labeler - Adventure Ready Brands (064437304)

Registrant - Adventure Ready Brands (064437304)

Establishment
Name	Address	ID/FEI	Business Operations
Adventure Ready Brands		064437304	manufacture(90107-2410)