Anti-Itch Spray

Manufacturer
Wakefern Food Corp | Vi-Jon
Effective date
2017-10-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:25

Label at a glance#

ProductDiphenhydramine HCl, Zinc Acetate
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE
Label structure8 sections

Indications and uses

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

Dosage and administration

•do note 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

Storage and handling

• store at 20⁰ - 25⁰C (68⁰ - 77⁰F)

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: iv, oak, sumac

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire of 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 into 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 note 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

STORAGE AND HANDLING SECTION

• store at 20⁰ - 25⁰C (68⁰ - 77⁰F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

*Not manufactured or distributed by Johnson + Johnson Consumer Products Company, distributor of Benadryl Spray

Distributed by: Wakefern Food Corporation

5000 riverside Drive, Keasbey, NJ 08832 (c) 2010

1-800-SHOPRITE www.shoprite.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TEAR HERE
Compare to the active ingredients in Benadryl Spray*
ShopRite

Itch Relief Spray

Topical analgesic/skin protectant

Extra strength/blocks hisitamine

Relieves pain and itching due to insect bites, poison ivy, oak, sumac, other minor skin irritations

2 FL OZ (59 mL)

image of principal display panelimage of principal display panel

295.000/295AB

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41190-29541190-295-16

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5256200f-8f09-4bd5-98ba-06d768310d9b02366463-afb8-439d-a20f-4ccd17c8c0ec2023-10-19WarningsExact identifier
spl set id: 02366463-afb8-439d-a20f-4ccd17c8c0ec

Reported adverse events (FAERS/openFDA)#

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