Label: TINTURA DE ARNICA- isopropyl alcohol and arnica extract solution

  • NDC Code(s): 70242-129-01
  • Packager: Dannso Corp./d.b.a. Essential Products
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2023

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

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredients                                                   Purpose

    Isopropyl Alcohol 63-69% by Volume................... Antiseptic

  • PURPOSE

    Use

    May help prevent skin infection in

    • minor cuts
    • scrapes 
    • burns
    • bruises
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    Antiseptic

    For External Use Only

  • DOSAGE & ADMINISTRATION

    Directions

    • clean the affected area
    • and dry thoroughly. Apply a thin layer 1 to 3 times daily.
    • May be covered with a sterile bandage, let dry first.
  • WARNINGS

    Warnings For external use only

    Avoid Contact with eyes.

    When using this product

    • do not use on irritated skin, in or near eyes or mocous membranes, on wounds or damaged skin, if prone to allergic reaction
    • Fatal if swallowed.

    Stop use and ask a doctor if condition persists or gets worse

  • INACTIVE INGREDIENT

    Inactive Ingredients Arnica Extract, Isopropyl Alcohol, Deionized Water

  • PRINCIPAL DISPLAY PANEL

    label image

  • INGREDIENTS AND APPEARANCE
    TINTURA DE ARNICA 
    isopropyl alcohol and arnica extract solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70242-129
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.13 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70242-129-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/08/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01401/01/2015
    Labeler - Dannso Corp./d.b.a. Essential Products (059741071)
    Registrant - Dannso Corp./d.b.a. Essential Products (059741071)
    Establishment
    NameAddressID/FEIBusiness Operations
    World Perfume, Inc101312044MANUFACTURE(70242-129)
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!