ITCH RELIEF- diphenhydramine hcl and zinc acetate spray 
Wal-Mart Stores, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Equate Itch Relief Pump Spray

Active ingredients

Diphenhydramine HCl 2.0%,

​Purpose

Topical Analgesic

​Uses

for the temporary relief of pain and itching associated with:

Warnings

For external use only.

Flammable:

Keep away from fire or flame.

​Do not use

  • on large areas of the body
  • on chicken pox, poison ivy, or sunburn
  • on broken, blistered, or oozing skin
  • more often than directed
  • with any other product containing diphenhydramine, even one taken by mouth

​When using this product

  • avoid contact with the eyes

​Stop use and ask doctor if

  • conditions worsens
  • symptoms persist for 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

​Other information

​Inactive ingredients

SD ALCOHOL 40-B, WATER, GLYCERIN, CAMPHOR, TROMETHAMINE, PVP, ALOE BARBADENSIS LEAF JUICE

​Questions?

1-888-287-1915

​Principal Display Panel

Equate

Extra Strength
Itch Relief

Pump Spray

Diphenhydramine

Hydrochloride 2%/

External Analgesic

Ozone-Friendly, Non-Aerosol

2.5 FL. OZ. (74mL)

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ITCH RELIEF 
diphenhydramine hcl and zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-217
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
POVIDONE (UNII: FZ989GH94E)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
TROMETHAMINE (UNII: 023C2WHX2V)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-217-2574 mL in 1 BOTTLE; Type 0: Not a Combination Product08/28/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM01708/28/2023
Labeler - Wal-Mart Stores, Inc. (051957769)

Revised: 8/2023
Document Id: 03feaade-963d-d473-e063-6294a90a4f09
Set id: 03feaaef-7401-d464-e063-6294a90a2b2d
Version: 1
Effective Time: 20230828
 
Wal-Mart Stores, Inc.