Label: EXTRA STRENGTH ITCH RELIEF- diphenhydramine hcl and zinc acetate spray

  • NDC Code(s): 83324-302-27
  • Packager: Chain Drug Marketing Association Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

If you are a consumer or patient please visit this version.

  • 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:

    • minor burns
    • sunburn
    • minor cuts
    • scrapes
    • insect bites
    • minor skin irritations
    • rashes due to poison ivy, poison oak and poison sumac
    • dries the oozing and weeping of poison ivy, poison oak and poison sumac
  • ​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

    • do not use more often than directed
    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • ​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

  • INGREDIENTS AND APPEARANCE
    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)