Itch Eraser Spray

Manufacturer: Tender Corporation d/b/a Adventure Ready Brands | Filltech USA, LLC
Effective date: 2025-11-18
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:16:35

Label at a glance#

ProductItch Eraser

Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE

Label structure8 sections

Indications and uses

For the temporary relief of pain and itching associated with, minor burns, sunburn,minor cuts, insects bites, minor skin irritations, rashes due to poison ivy, poison oak, and poison sumac

Dosage and administration

Shake before use remove safety tab from spray head 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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Diphenhydramine HCl 2%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain and itching associated with, minor burns, sunburn,minor cuts, insects bites, minor skin irritations, rashes due to poison ivy, poison oak, and poison sumac

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

Ask a doctor before use

OTC - ASK DOCTOR SECTION

on chicken ox, measles

when using this product

OTC - WHEN USING SECTION

avoid contact with eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worses, if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake before use

remove safety tab from spray head

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

INACTIVE INGREDIENT SECTION

glycerinm oat beta glucanm povidone, purified water, sd alcohol 40-2, sodium bicarbonate (baking soda), tea tree oil, vitamine e acetate, zinc acetate

Itch Eraser Spray Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary Packaging

Itch Eraser Spray Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secondary Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1050080	diphenhydrAMINE HCl 2 % Topical Spray	PSN	2
1724486	The Itch Eraser 2 % Topical Spray	PSN	2
1724486	diphenhydramine hydrochloride 20 MG/ML Topical Spray [The Itch Eraser]	SBD	2
1050080	diphenhydramine hydrochloride 20 MG/ML Topical Spray	SCD	2
1050080	diphenhydramine HCl 2 % Topical Spray	SY	2
1724486	The Itch Eraser 2 % Topical Spray	SY	2
1724486	The Itch Eraser 20 MG/ML Topical Spray	SY	2

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
DIPHENHYDRAMINE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0044224624109	GTIN-13: 0044224624109 EAN-13: 0044224624109 GTIN-12: 044224624109 UPC-A: 044224624109 GTIN storage (14 digits): 00044224624109	Itch eraser Spray Box.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44224-1114-0	Itch Eraser	25.5 g in 1 BOTTLE, SPRAY	SPRAY	25.5		2
44224-1114-1	Itch Eraser	1 in 1 BOX	SPRAY	1		2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

Itch Eraser
Diphenhydramine HCl
TEA TREE OIL
POVIDONE K30
WATER
OAT
ZINC ACETATE
SODIUM BICARBONATE
.ALPHA.-TOCOPHEROL ACETATE
GLYCERIN
DIPHENHYDRAMINE HYDROCHLORIDE
DIPHENHYDRAMINE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
44224-1114	44224-1114-0, 44224-1114-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TEA TREE OIL	VIF565UC2G	IACT
POVIDONE K30	U725QWY32X	IACT
WATER	059QF0KO0R	IACT
OAT	Z6J799EAJK	IACT
ZINC ACETATE	FM5526K07A	IACT
SODIUM BICARBONATE	8MDF5V39QO	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
GLYCERIN	PDC6A3C0OX	IACT
DIPHENHYDRAMINE HYDROCHLORIDE	TC2D6JAD40	ACTIB
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Itch Eraser	DIPHENHYDRAMINE HCL	Tender Corporation d/b/a Adventure Ready Brands	2204e135-6a23-68a2-e063-6394a90ac019	2025-11-18	Warnings	Exact identifier ndc (package): 44224-1114-1 ndc (package): 44224-1114-0 ndc (product): 44224-1114 ndc11 (package): 44224111400 ndc11 (package): 44224111401 spl id: 43e0123a-989b-6eb9-e063-6394a90a40dc spl set id: 2204e135-6a23-68a2-e063-6394a90ac019

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.