Label: SANITIZE ASAP HAND SANITIZER- isopropyl 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 April 6, 2020

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

View All Sections
  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient:

    Isopropyl Alcohol 70%

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses: to decrease bacteria on the skin that could interfere with good health, recommended for repeated use. 

  • WARNINGS

    Warnings

    Flammable, keep away from heat and flame.

    Keep out of reach of children, keep out of the eyes, avoid contact with broken skin, if swallowed get medical help or contact a poison control center. 

  • DOSAGE & ADMINISTRATION

    Directions: wet the hands thoroughly with the product and allow to dry without wiping.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Alcohol, Deionized water, Hydroxypropyl guar, Eucalyptus globulus

  • SPL UNCLASSIFIED SECTION

    ANTI-BACTERIAL

    KILLS 99.99% OF GERMS

    MADE IN USA

    LABORATORY CRAFTED - ANTI-BACTERIAL BLEND FROM THE RESEARCH LABORATORIES OF NWH. 

    BE SAFE  BE CAUTIOUS

    SANITIZEASAP.COM

    New World Cosmetics and Medicinals.

    1080 Holland Drive. Suite 1

    Boca Raton, Florida 33487

    These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat cure or prevent any disease.

  • Packaging

    asap1

    asap-2

  • INGREDIENTS AND APPEARANCE
    SANITIZE ASAP HAND SANITIZER 
    isopropyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73871-377
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    GUARAPROLOSE (3500 MPA.S AT 1%) (UNII: 3A1I7376TC)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73871-377-6060 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/18/2020
    2NDC:73871-377-24236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/18/2020
    3NDC:73871-377-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/18/2020
    4NDC:73871-377-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/18/2020
    Labeler - New World Holdings, Inc. (081183610)
    Establishment
    NameAddressID/FEIBusiness Operations
    New World Holdings, Inc.081183610manufacture(73871-377)
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!