Itch Relief

Manufacturer
Vi-Jon, LLC
Effective date
2022-04-25
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 22:02:39

Label at a glance#

ProductItch Relief
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE
Label structure14 sections

Indications and uses

for the temporary relief of pain and itching associated with ■ insect bites ■ minor skin irritations ■ sunburn ■ minor burns ■ minor cuts ■ scrapes ■ rashes due to poison: ■ ivy ■ oak ■ sumac 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 ■ insect bites ■ minor skin irritations ■ sunburn
    ■ minor burns ■ minor cuts ■ scrapes ■ rashes due to poison: ■ ivy ■ oak ■ sumac
  • 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 ■ on 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
■ 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

Adverse Reactions 

ADVERSE REACTIONS SECTION

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

Manufactured by: Vi-Jon, LLC

St. Louis, MO 63114

Questions or comments?  1-888-593-0593

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mountain Falls

*Compare to Benadryl

Itch Relief Spray

topical analgesic

skin protectant

Made in the USA with US and foreign parts.

2 FL OZ (59 mL)

image descriptionimage description

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
0869-02950869-0295-20

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
10459e81-5432-9ce5-e063-6394a90a5687951eb793-a113-46f1-b8ea-c3828d27e05d2024-01-31Warnings, Adverse reactionsExact identifier
spl set id: 951eb793-a113-46f1-b8ea-c3828d27e05d

Reported adverse events (FAERS/openFDA)#

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