Label: FB HYDRATING HAND SANITIZER gel

  • NDC Code(s): 75541-011-01
  • Packager: NINGBO MEITELI COSMETICS CO., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 13, 2024

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

View All Sections
  • Active Ingredient(s)

    ETHYL ALCOHOL：70%

  • Purpose

    Antiseptic

  • Use

    hand sanitizer to help reduce bacteria on the skin.

  • Warnings

    Flammable: Keep away from fire or flame.
    For external use only.

  • Do not use

    Children under two years old, please do not use

  • WHEN USING

    When using this product keep out of eyes, ears and mouth.
    In case of contact, rinse eyes thoroughly with water.
    Avoid contact with broken skin.

  • STOP USE

    Stop use and see a doctor if irritation or rash appears and lasts.

  • 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.

  • Directions

    Spray enough sanitizer in your palm to cover both hands. Rub hands
    together briskly until dry. Children under six should be supervised.

  • Other information

    Protect the product in this container from excessive heat and direct sun.
    Store below 104 0F (40 0C).
    May discolor certain fabrics.

  • Inactive ingredients

    Water, Glycerin, Fragrance, Red 40 Lake (CI 16035), Red 33 (CI 17200)

  • Package Label - Principal Display Panel

    label

  • INGREDIENTS AND APPEARANCE
    FB HYDRATING HAND SANITIZER 
    fb hydrating hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75541-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEHYDRATED ALCOHOL (UNII: 3K9958V90M) (DEHYDRATED ALCOHOL - UNII:3K9958V90M) DEHYDRATED ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75541-011-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product05/13/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00505/13/2024
    Labeler - NINGBO MEITELI COSMETICS CO., LTD (546624772)
    Establishment
    NameAddressID/FEIBusiness Operations
    NINGBO MEITELI COSMETICS CO., LTD546624772manufacture(75541-011)
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!