ITCH RELIEF- diphenhydramine hcl, zinc acetate spray 
The Kroger Co

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Kroger Itch Relief Spray
295.000/295AA-AB

Active ingredients

Diphenhydramine HCl 2%

Zinc acetate 0.1%

Purpose

External analgesic

Uses

Warnings

For external use only

Flammable, Keep away from fire or flame.

Do not use

Ask a doctor before use

on chicken pox or measles

When using this product

do not get into eyes

Stop use and ask a doctor if

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.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

do not use more than directed

Other

store at 20º to 25º C (68º to 70ºF)

Inactive ingredients

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

Questions?

1-800-632-6900

Adverse reaction

DISTRIBUTED BY THE KROGER CO.CINCINNATI, OHIO 45202

disclaimer

Benadryl® is a registered trademark of Kenvue, Inc. Kenvue, Inc. is not affiliated with The Kroger Co. or this product.

Principal display panel

TEAR HERE

NDC 59450-295-20

COMPARE TO the active ingredients in BENADRYL ® EXTRA STRENGTH TOPCICAL ANALGESIC SPRAY*

Kroger ®

Extra Strength

Itch Relief Spray

Diphenhydramine HCI 2%

Topcail Analgesic

Zinc Acetone 0.1%

Skin Protectant

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

2 FL OZ (59 mL)

mm01

ITCH RELIEF 
diphenhydramine hcl, zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59450-295
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 mL
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
POVIDONE (UNII: FZ989GH94E)  
TROMETHAMINE (UNII: 023C2WHX2V)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59450-295-2059 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/02/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01602/02/2024
Labeler - The Kroger Co (006999528)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(59450-295)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091520manufacture(59450-295)

Revised: 3/2024
Document Id: 13f4a348-7edc-2016-e063-6394a90a6e9e
Set id: 106a2968-444a-e77d-e063-6394a90aa8c3
Version: 2
Effective Time: 20240318
 
The Kroger Co