Label: HAND SANITIZER- ethyl alcohol gel

  • 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 November 5, 2020

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients

    Ethyl Alcohol

  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    Lovercare Healthy care ANTIBACTERIAL HAND SANITIZER is formulated to help neutralise & remove bacteria effectively.

  • DOSAGE & ADMINISTRATION

    INSTRUCTIONS:

    First rotate nozzle anti-clockwise to open & then press pump to allow product to dispense. Apple a generous amount to the palm. Spread and rub over back of hands and finger tips. Allow hands to air dry.

  • WARNINGS

    Caution:

    Highly flammable. For external use only.

  • WHEN USING

    Do not ingest. Avoid eyes.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • KEEP OUT OF REACH OF CHILDREN

    If irrtation occurs, wash affected area and discontinue use.

  • OTHER SAFETY INFORMATION

    Do not use on inflamed, broken or sensitive skin. Store below 30℃. For advice, contact a Poisons Information Centre (AUS: 13 11 26), or a doctor.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Water,Carbomer 940,Triethanolamine,Glycerin,Aloe Barbadensis leaf juice,Vitamin E,Fragrance,CI19140,CI42090.

  • PRINCIPAL DISPLAY PANEL

    image of hand sanitizer 55mlimage of hand sanitizer 60mlimage of hand sanitizer 240ml

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47993-288
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 112 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    TRIETHANOLAMINE BENZOATE (UNII: M3EN4GC19W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47993-288-0155 mL in 1 BOTTLE; Type 0: Not a Combination Product06/24/2020
    2NDC:47993-288-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product06/24/2020
    3NDC:47993-288-03240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/24/2020
    Labeler - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)
    Registrant - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)
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!