ITCH RELIEF GEL- diphenhydramine hcl gel 
Walgreens

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Walgreens Itch Relief Gel

Active ingredient

Diphenhydramine HCL 2%

Purpose

Topical Analgesic

Use

Temporarily relieves pain and itching associated with: insect bites, minor burns, sunburn, minor cuts, scrapes, minor skin irritations, rashes due to poison ivy, poison oak, and poison sumac

Warnings

For external use only.

Do not use:

on large areas of the body,

with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use 

on chicken pox,

on measles

When using this product

avoid contact with eyes

Stop use and ask a doctor if

condition 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

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.

Other information

Store at room temperature

Inactive ingredients

camphor, diazolidinyl urea, glycerin, hydroxypropyl methylcellulose, methylparaben, propylene glycol, propylparaben, purified water, SD alcohol 40-B, sodium citrate

Questions?

1-800-925-4733

Directions

Apply to affected area not more thatn 3 to 4 times daily

Tube label

Tube label

ITCH RELIEF GEL 
diphenhydramine hcl gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0353
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
ALCOHOL (UNII: 3K9958V90M)  
HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)  
Product Characteristics
Colorwhite (clear) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0353-04103.5 mL in 1 TUBE; Type 0: Not a Combination Product05/30/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/30/2018
Labeler - Walgreens (008965063)
Registrant - Unipack LLC (116015769)
Establishment
NameAddressID/FEIBusiness Operations
Unipack LLC009248480manufacture(0363-0353)

Revised: 2/2024
Document Id: 1210e28e-7628-f6e5-e063-6394a90a6108
Set id: 487060a7-dff3-4840-b967-ca919f8d0a29
Version: 5
Effective Time: 20240223
 
Walgreens