DIPHENHYDRAMINE HCL AND ZINC ACETATE- extra strength itch relief continuous spray aerosol, spray 
Topco Associates LLC

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TOPCARE Itch Relief Continous Spray

Active Ingredients

Diphenhydramine HCL 2.0%

Zinc Acetate 0.1%

Purpose

External analgesic

Skin Protectant

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 120 ºF

Intentional misuseby 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

  • 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.

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 1-888-423-0139

Principal Display Panel

TopCare health

EXTRA STRENGTH

Itch Relief Continous Spray

DIPHENHYDRAMINE HYDROCHLORIDE 2%

EXTERNAL ANALGESIC

ZINC ACETATE 0.1%

SKIN PROTECTANT

NET WT 2.7 OZ (76g)

topcare itch relief spray

DIPHENHYDRAMINE HCL AND ZINC ACETATE 
extra strength itch relief continuous spray aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-126
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE1.5 g  in 76 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.075 g  in 76 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALCOHOL (UNII: 3K9958V90M)  
TROMETHAMINE (UNII: 023C2WHX2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36800-126-7676 g in 1 CANISTER; Type 0: Not a Combination Product03/05/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/05/2019
Labeler - Topco Associates LLC (006935977)

Revised: 2/2024
Document Id: 10e0d64a-7141-5834-e063-6294a90a9e53
Set id: 8026c7dd-eb7b-ebea-e053-2991aa0a1b0f
Version: 5
Effective Time: 20240208
 
Topco Associates LLC