Label: IC IVY RELIEF- diphenhydramine hydrochloride and zinc acetate liquid

  • NDC Code(s): 59555-230-04, 59555-230-07, 59555-230-18, 59555-230-19
  • Packager: R & R Lotion, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 24, 2021

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active IngredientsPurpose
    Diphenhydramine HCL 2%Topical Analgesic
    Zinc Acetate 0.1%Skin Protectant
  • Uses

    Temporary relieves pain and itching associated with: Insect Bites

    • Minor Burns
    • Minor Cuts
    • Sunburn
    • Minor Skin Irritations
    • Scrapes
    • Dries oozing and weeping of Poison Ivy, Poison Oak, and Poison Sumac
    • Rashes due to Poison Ivy, Poison Oak, and Poison Sumac.
  • Warnings

    For external use only. Do not use on large areas of the body

    • with any other product containing diphenhydramine, even one taken by mouth.

    Ask doctor before use on chicken pox

    • on measles

    When using this product avoid contact with eyes

    Stop use and ask doctor if conditions worsen, or do not improve within 7 days

    • symptoms persist for 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 Poison Control Center right away.

  • Directions

    Do not use more than directed

    • Hold stick straight down over infected area
    • press tip of stick repeatedly on affect skin area until liquid flows, then dab sparingly
    • adults and children 2 years of age and older: apply to affected area not more then 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • Other Information

    Protect from excessive heat (40ºC/104ºF)

  • Inactive Ingredients

    Propylene Glycol, Xanthan Gum, DI Water, PVP K-30

  • Questions or Comments?

    1-888-860-7424

  • PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label

    I.C.®
    Ivy
    Relief

    R&R LOTION
    USA

    Kills Germs

    2oz. (59ml) ℮

    PRINCIPAL DISPLAY PANEL - 59 ml Bottle Label
  • INGREDIENTS AND APPEARANCE
    IC IVY RELIEF 
    diphenhydramine hydrochloride and zinc acetate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59555-230
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 mL
    Zinc Acetate (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) Zinc Acetate1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    POVIDONE K30 (UNII: U725QWY32X)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59555-230-181 mL in 1 PACKET; Type 0: Not a Combination Product09/01/2021
    2NDC:59555-230-1920 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product09/01/2021
    3NDC:59555-230-0459 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2021
    4NDC:59555-230-07118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34809/01/2021
    Labeler - R & R Lotion, Inc (062979000)