ITCH RELIEF- diphenhydramine hydrochloride, zinc acetate cream 
CVS Pharmacy

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CVS Pharmacy, Inc. Itch Relief Cream Drug Facts

Active ingredients

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

Principal Display Panel

Compare to the active ingredients in Extra Strength Benadryl® Itch Stopping Cream

EXTRA STRENGTH

Itch Relief Cream

DIPHENHYDRAMINE HYDROCHLORIDE 2% / ZINC ACETATE 0.1%

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 (28 g)

Package Contains One Tube

itch-relief.jpg
ITCH RELIEF 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-708
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)  
PEG-2 STEARATE (UNII: 94YQ11Y95F)  
PEG-20 STEARATE (UNII: NBX892EA57)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-708-641 in 1 CARTON06/08/2005
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 DrugM01706/08/2005
Labeler - CVS Pharmacy (062312574)

Revised: 10/2023
Document Id: d3a43dc1-7ece-4cee-88ed-52238abd5a64
Set id: 0e988da1-1904-431d-a152-bdb2aacc8e16
Version: 11
Effective Time: 20231013
 
CVS Pharmacy