Label: IVY-DRY SUPER- benzyl alcohol, camphor, menthol spray

  • 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 December 27, 2017

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

View All Sections
  • Active Ingredients

    Benzyl Alcohol 10%

    Camphor 0.5%

    Menthol 0.25%


    Purpose

    External Analgesic


  • Uses

    • for the temporary relief of itching associated with insect bites and minor skin irritations
  • WARNINGS

    For external use only.

    Do not use

    • on face or genital areas
    • on areas of blistered or broken skin
    • with a compress after application

    When using this product

    • do not get into eyes
    • if contact occurs, flush eyes with water

    Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days.

    If pregnant or breast-feeding,

    ask a doctor before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    • Apply to affected area not more than 3 times daily.
    • Children under 6 years of age: do not use, ask a doctor.
    • Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary.
    • Test product on small patch of skin before applying to the entire body.
  • Other information

    Store at room temperature

    You may report a serious adverse reaction to Report Reaction LLC, PO Box 22, Plainsboro, NJ 08536-0222


  • Inactive Information

    WATER, ISOPROPANOL, ZINC ACETATE, ISOCETETH-20, ZINC LACTATE

  • Package Labeling


    Ivy-Dry Super

    TEMPORARY RELIEF OF PAIN AND ITCHING
    Associated with Minor Skin Irritations and Insect Bites

    External Analgesic


    Manufactured in the USA for:
    Ivy-Dry, Inc.
    299-B Fairfield Avenue
    Fairfield, NJ 07070

    ©2012 Ivy-Dry, Inc.

    Questions or Comments www.ivydry.com



    Ivy-Dry Super

  • INGREDIENTS AND APPEARANCE
    IVY-DRY SUPER 
    benzyl alcohol, camphor, menthol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49546-106
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL100 mg  in 1 mL
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)5 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ZINC ACETATE (UNII: FM5526K07A)  
    ISOCETETH-20 (UNII: O020065R7Z)  
    ZINC LACTATE (UNII: 2GXR25858Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49546-106-06177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/21/2012
    Labeler - Ivy-Dry, Inc. (800544590)
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!