DIPHENHYDRAMINE HCL AND ZINC ACETATE- extra strength itch relief spray 
Discount Drug Mart

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Discount Drug Mart Itch Relief Continuous Spray

Active ingredients

Diphenhydramine HCl 2.0%
Zinc Acetate 0.1%

Purpose

Uses

for temporary relief of pain and itching associated with:

Flammable:

Keep away from fire or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.

Do not use

  • on large areas of the body
  • with any other products containing diphenhydramine, even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • on measles

Stop use and ask doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

When using this product

  • avoid contact with eyes
  • use only as directed

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

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Extra Strength

Itch Relief

CONTINUOUS SPRAY

Diphenhydramin Hydrochloride 2%/ External Analgesic

Zinc Acetate 0.1%/ Skin Protectant

NET WT 2.7 OZ (76 g)

DM Itch Relief Spray_50-082DD-01.jpg

DIPHENHYDRAMINE HCL AND ZINC ACETATE 
extra strength itch relief spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53943-030
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE1.52 g  in 76 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.076 g  in 76 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53943-030-7676 g in 1 CAN; Type 0: Not a Combination Product03/25/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/25/2013
Labeler - Discount Drug Mart (047741335)

Revised: 1/2024
Document Id: 0fb88daa-3dd9-e097-e063-6394a90a8a5c
Set id: d4ef917b-a9a8-4102-97d3-d7233393e622
Version: 5
Effective Time: 20240124
 
Discount Drug Mart