Label: ALCOHOL HAND SANITIZER- alcohol 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 January 4, 2022

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

View All Sections
  • Directions:

    Spray enough product on hands to cover all surfaces. Rub hands together until dry.

  • Active Ingridient

    Ethyl Alcohol (62%).

  • Inactive Ingredients:

    Deionized Water, Glycerin, Propylene Glycol, Tocopherol, Citrus Fragrance, Aloe Vera.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DO NOT USE

    Do not use on children less than 2 months of age. Do not use on open skin wounds.

  • WARNINGS

    For external use only. Flammable. Keep away from heat or flame. Keep out of eyes, eras & mouth. In case of contact with eyes, rinse eyes thoroughly with water. If swallowed, get medical help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    Antibacterial hand sanitizer spray.

  • PURPOSE

    Antiseptic.

  • PRINCIPAL DISPLAY PANEL

    4OZAN-page-001

  • INGREDIENTS AND APPEARANCE
    ALCOHOL HAND SANITIZER 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70445-412
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70445-412-2060 mL in 1 BOTTLE; Type 0: Not a Combination Product05/08/2020
    2NDC:70445-412-22120 mL in 1 BOTTLE; Type 0: Not a Combination Product05/08/2020
    3NDC:70445-412-2310 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    4NDC:70445-412-2620 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    5NDC:70445-412-215 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/08/2020
    Labeler - Webb Business Promotion (154445647)
    Establishment
    NameAddressID/FEIBusiness Operations
    Webb Business Promotion154445647manufacture(70445-412)
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!