CVS ITCH RELIEF- diphenhydramine hcl, zinc acetate spray 
CVS

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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CVS Extra Strength Itch Relief Spray

Active Ingredient

Diphenhydramine hydrochloride 2% Topical analgesic

Zinc acetate 0.1% Skin protectant

Uses

for

temporary relieves pain and itching due to:

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

oak

sumac

Directions

do not use more often than directed

adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily

children under 2 years: ask a doctor

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 doctor Before use

on chicken pox

on measles

When using this product

do not get into eyes

Stop Use and ask physician

condition worsens

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.

Warning

for external use only

Purposes

Itch relief

Inactive Ingredients

Purified Water, Glycerin, SD Alcohol, Povidone, Povidonee (K-30), Trolamine

Prinicpal dispaly panel

CVS itch spray .jpg

Diphenhydramine hydrochloride 2%

Topical analgesic

Zinc acetate 0.1% Skin protectant

Relieves Itch and Pain associated with insects bites & rashes due to posinon ivy Oak& sumac

CVS ITCH RELIEF 
diphenhydramine hcl, zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-952
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 mL
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALCOHOL (UNII: 3K9958V90M)  
POVIDONE K30 (UNII: U725QWY32X)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-952-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/14/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/14/2014
Labeler - CVS (062312574)
Registrant - Weeks & LEO, Inc. (005290028)
Establishment
NameAddressID/FEIBusiness Operations
Weeks & Leo005290028manufacture(69842-952)

Revised: 4/2019
Document Id: 8723bb57-31e5-54d6-e053-2a91aa0a3e90
Set id: 8723e097-296f-784a-e053-2991aa0a552e
Version: 1
Effective Time: 20190422
 
CVS