EXTRA STRENGTH ITCH RELIEF- diphenhydramine hcl and zinc acetate spray 
Chain Drug Marketing Association Inc

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Quality Choice Itch Relief Continuous Spray

Active ingredients

Diphenhydramine HCl 2.0%,

Zinc acetate 0.1%

​Purpose

​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 puncture or incinerate. Contents under pressure. Do not store at temperatures above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

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 doctor if

  • conditions 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.

Directions

​Other information

store between 20° to 25°C (68° to 77°F)

​Inactive ingredients

aloe barbadensis leaf juice, glycerin, purified water, SD alcohol 40-B, tromethamine

​Questions?

call 1-866-964-0939

Principal Display Panel

QC

CONTINUOUS

CHOICE

Extra Strength

Itch Relief

Continous

Spray

Diphenhydramine Hydrochloride 2% /

External Analgesic


Zinc Acetate 0.1% /

Skin Protectant

Relieves itching from insect

bites and poison ivy, oak &

sumac

Soothes sunburn and

minor burns & cuts

NET WT. 2.7 OZ. (76 g)

label

EXTRA STRENGTH ITCH RELIEF 
diphenhydramine hcl and zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-302
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALCOHOL (UNII: 3K9958V90M)  
TROMETHAMINE (UNII: 023C2WHX2V)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-302-2776 g in 1 CAN; Type 0: Not a Combination Product06/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/06/2024
Labeler - Chain Drug Marketing Association Inc (011920774)

Revised: 11/2025
Document Id: 42f3fe19-b76d-2a12-e063-6394a90afd7f
Set id: 1a2997bc-7741-e658-e063-6394a90af6fd
Version: 3
Effective Time: 20251106
 
Chain Drug Marketing Association Inc