Label: BYE BYE GERMS OMG ALL PURPOSE SANITIZING- 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 April 24, 2020

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

View All Sections
  • Active ingredient

    Ethyl alcohol 62% v/v

  • Purpose

    Antimicrobial

  • Use

    • To decrease bacteria
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

    Keep out of reach of children.

  • Other information

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces
  • Directions

    Perfectly Sanitize Instantly!
    Wet hands thoroughly with product and allow to dry without wiping
    Travel-friendly. Don't leave home without it!

  • Inactive ingredients

    Water (Aqua), Polysorbate 20, Tocopheryl QAcetate, Aloe Barbadensis Leaf Extract

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    BYE BYE GERMS OMG ALL PURPOSE SANITIZING 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73724-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73724-002-0150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/26/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/26/2020
    Labeler - JK BEAUTY GROUP, INC. (066536143)
    Registrant - JK BEAUTY GROUP, INC. (066536143)
    Establishment
    NameAddressID/FEIBusiness Operations
    BEAUTY SKIN.CO.,Ltd.688530942manufacture(73724-002)
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!