ITCH RELIEF- diphenhydramine hydrochloride, zinc acetate cream 
H E B

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HEB Itch Relief Cream Drug Facts

Active ingredient

Diphenhydramine hydrochloride 2%

Zinc acetate 0.1%

Purpose

Topical analgesic

Skin protectant

Uses

•
temporarily relieves pain and itching associated with:
•
insect bites
•
minor burns
•
sunburn
•
minor skin irritations
•
minor cuts
•
scrapes
•
rashes due to poison ivy, poison oak and poison sumac
•
dries the oozing and weeping of 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 the eyes

Stop use and ask a doctor if

•
condition worsens or does not improve within 7 days
•
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 no more than 3 to 4 times daily
•
children under 2 years of age: ask a doctor

Other information

•
store at 20°-25°C (68°-77°F)

Inactive ingredients

cetyl alcohol, diazolidinyl urea, methylparaben, PEG-2 stearate, PEG-20 stearate, propylene glycol, propylparaben, purified water

Questions or comments?

1-800-719-9260

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Compare to active ingredients in Extra Strength Benadryl® Cream

Extra Strength

H-E-B®

Itch Relief Cream

2% DIPHENHYDRAMINE HCl and 0.1% ZINC ACETATE

Topical Analgesic & Skin Protectant

Temporary Relief of Itch and Pain due to:

• Insect Bites • Minor Skin Irritations • Rashes from Poison Ivy, Poison Oak or Poison Sumac

NET WT. 1 OZ (28g)

HEB ITCH RELIEF CREAM CARTON IMAGE
ITCH RELIEF 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-622
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-622-641 in 1 CARTON09/15/2010
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01709/15/2010
Labeler - H E B (007924756)

Revised: 10/2024
Document Id: 73bec294-055a-4342-9cdf-00cd83e1d0ad
Set id: 34c7bcd3-203f-4630-894d-3739a1576c8d
Version: 3
Effective Time: 20241013
 
H E B