Label: ITCH STOPPING CREAM- diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream

  • NDC Code(s): 69396-150-01
  • Packager: Trifecta Pharmaceuticals USA, LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 12, 2024

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

View All Sections
  • Active Ingredient

    Diphenhydramine Hydrochloride 2%

  • Purpose

    Topical Analgesic

  • Active Ingredient

    Zinc Acetate 0.1%

  • Purpose

    Skin Protectant

  • INDICATIONS & USAGE

    Temporarily relieves pain and itching associated with

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

    For External Use Only

  • Do Not Use

    Do Not Use on large areas of the body or with any other product containing diphenhydramine, even one taken by mouth.

  • When Using this product

    When Using this Product avoid contact with Eyes

  • Stop Use and Ask a Doctor If

    Stop Use and Ask a Doctor if

    • Conditions worsen or do not improve within 7 days
    • Symptoms presist for more than 7 days or clear up and occur again within a few days
  • Keep out of the reach of children

    If swallowed, get medical help or contact a Poison Control Center immediately

  • Ask a Doctor before Use

    Ask a doctor before use on chicken pox or measles

  • Directions

    • Do not use more 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: consult a doctor
  • Other information

    • Store at controlled room temperature 20º-25ºC (68º-77ºF)
    • Close cap tightly after use

  • Inactive Ingredients

    Aloe Barbadensis leaf juice, Cetyl alcohol, Glyceryl monostearate, Methylparaben, Mineral Oil, Petrolatum, Polyoxyethylene lauryl ether, Propylene glycol, Propylparaben, Purified Water, Stearic acid

  • Distributed By:

    Proudly Distributed by Associated Wholesale Grocers Inc.

    Kansas City, KS. 66106 USA

    Questions Call: 1-877-753-3935

    Monday-Friday 9AM-5PM EST

    This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., owner of the registered trademark Extra Strength Benadryl® Itch Stopping Cream.

    00000 Rev0000000000

  • Packaging

    Best Choice Itch Stopping Cream 1oz 040523 CDER

  • INGREDIENTS AND APPEARANCE
    ITCH STOPPING CREAM 
    diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-150
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LAURETH-23 (UNII: N72LMW566G)  
    WATER (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69396-150-011 in 1 BOX11/29/2023
    128.3 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/29/2023
    Labeler - Trifecta Pharmaceuticals USA, LLC. (079424163)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!