FDA.reportPublic FDA data

Meijer 295.000/295AA-AB Itch Relief Spray

Manufacturer
Meijer, Inc. | Nice-Pak Products, LLC
Effective date
2026-02-19
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-06-01 01:46:43

Label at a glance#

ProductItch Relief
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE
Label structure15 sections

Indications and uses

for the temporary relief of pain and itching associated with minor skin irritations dries the oozing and weeping of poison: ivy, oak, sumac

Dosage and administration

do not use more 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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Diphenhydramine HCL 2%

Zinc acetate 0.1%

Purpose

OTC - PURPOSE SECTION

External analgesic

Skin protectant

Uses

INDICATIONS & USAGE SECTION

  • for the temporary relief of pain and itching associated with minor skin irritations
  • dries the oozing and weeping of poison: ivy, oak, sumac

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame.

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 pox or measles

When using this product

OTC - WHEN USING SECTION

do not get in eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or symptoms last 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 a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not use more 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

Other information

SPL UNCLASSIFIED SECTION

store at 20⁰ to 25⁰ C (68⁰ to 77⁰ F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol, glycerin, povidone, purified water, tris (hydroxymethyl)aminomethane

Disclaimer

SPL UNCLASSIFIED SECTION

*THIS PRODUCT IS NOT MANUFACTURED OR DISTRIBUTED BY KENVUE, INC., DISTRIBUTOR OF BENADRYL ®EXTRA STRENGTH SPRAY.

Adverse Reactions

ADVERSE REACTIONS SECTION

DIST. BY MEIJER DISTRIBUTION, INC.

GRAND RAPIDS, MI 49544

www.meijer.com

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 41250-295-20

TEAR HERE

COMPARE TO BENADRYL ®SPRAY ACTIVE INGREDIENTS*

meijer ®

Itch Relief Spray

TOPICAL ANALGESIC

SKIN PROTECTANT

Pain & Itch Reliever

2 FL OZ (59 mL)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1053138diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical SprayPSN14
1053138diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical SpraySCD14
1053138diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical SpraySY14

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIPHENHYDRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-295-20Itch Relief59 mL in 1 BOTTLE, SPRAYSPRAY5914

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-29541250-295-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
POVIDONEFZ989GH94EIACT
WATER059QF0KO0RIACT
TROMETHAMINE023C2WHX2VIACT
DIPHENHYDRAMINE HYDROCHLORIDETC2D6JAD40ACTIB
ZINC ACETATEFM5526K07AACTIB

Source Document#

Source XML · Source PDF

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Itch ReliefDIPHENHYDRAMINE HCL, ZINC ACETATEMeijer, Inc.e11390ec-99a3-4ff1-a3c8-ca909f4f67b52026-02-19Warnings, Adverse reactionsExact identifier
ndc (package): 41250-295-20
ndc (product): 41250-295
ndc11 (package): 41250029520
spl id: 4b329231-6e22-7c43-e063-6394a90a307a
spl set id: e11390ec-99a3-4ff1-a3c8-ca909f4f67b5

Reported adverse events (FAERS/openFDA)#

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