DIPHENHYDRAMINE HCL AND ZINC ACETATE- allergy relief spray aerosol, spray 
Chain Drug Consortium, LLC

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Premier Value Allergy Itch Relief Spray


Active ingredients

Diphenhydramine HCl 2%,
Zinc Acetate 0.1%

Purpose

Uses

for the temporary relief of pain and itching associated with:

Warnings

For external use only.

Flammable:

Do not use while smoking or near heat 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 product containing diphenhydramine, even one taken by mouth

​Ask a doctor before use

  • on chicken pox
  • on measles

Stop use and ask doctor if

  • conditions 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

Premier Value

Extra Strength
Allergy Relief Spray
Continuous Spray
Diphenhydramine HCl 2%,
Zinc Acetate 0.1%

Net Wt 2.7 OZ (76 g)

PV Allergy Relief Spray2.jpg

DIPHENHYDRAMINE HCL AND ZINC ACETATE 
allergy relief spray aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-631
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)  
TROMETHAMINE (UNII: 023C2WHX2V)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-631-0076 g in 1 CAN; Type 0: Not a Combination Product12/10/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/10/2010
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2024
Document Id: 1057cda0-76ee-f96b-e063-6294a90a8f3a
Set id: 7618bb67-0758-4db4-bbfd-f812b6708c5a
Version: 8
Effective Time: 20240201
 
Chain Drug Consortium, LLC