Label: VITAPLUS FORE- ethanol, titanium dioxide liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 15, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Ethanol, Titanium Dioxide

  • INACTIVE INGREDIENT

    Pinus densiflora callus extract ,Foeniculum vulgare seed extract,Indican,Maltitol,Sorbitol,Water

  • PURPOSE

    Antiseptic

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Do not dilute.• Use at strength for maximum effectiveness.• For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

  • WARNINGS

    Warnings

    For external use only.

    When using this product • Keep out of eyes • In case of contact with eyes, flush thoroughly with water.

    Stop use and ask a doctor ifirritation or redness develop and persist for more than 72 hours.

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

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    VITAPLUS FORE 
    ethanol, titanium dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71544-0022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.008 g  in 100 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.01 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)  
    INDICAN (UNII: N187WK1Y1J)  
    SORBITOL (UNII: 506T60A25R)  
    MALTITOL (UNII: D65DG142WK)  
    WATER (UNII: 059QF0KO0R)  
    FENNEL SEED (UNII: G3QC02NIE6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71544-0022-14000 mL in 1 DRUM; Type 0: Not a Combination Product04/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2021
    Labeler - MY Corp.,Ltd (688202781)
    Registrant - MY Corp.,Ltd (688202781)
    Establishment
    NameAddressID/FEIBusiness Operations
    MY Corp.,Ltd688202781manufacture(71544-0022) , label(71544-0022) , pack(71544-0022)
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!