Label: 5ML HAND SANITIZER- 5ml hand sanitizer spray 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 December 20, 2020

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

  • Active Ingredient(s)

    Ethyl alcohol 75%

  • Purpose

    Antiseptic

  • Use

    For handwashing to decrease bacteria on the skin

  • Warnings

    For external use only
    Flammable, keep away from fire or flame

  • Do not use

  • WHEN USING

    Do not use in the eyes
    Stop use and ask a doctor if
    irritation and redness develop
    condition persists for more than 72 hours

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if
    irritation and redness develop
    condition persists for more than 72 hours

  • 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

    Wet hands thoroughly with product and allow to dry wthout wiping

  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    Aloe vera leaf juice, glycerol, water.

  • Package Label - Principal Display Panel

    75273-007-01 5ml hand sanitizer spray

    75273-007-01 5ml hand sanitizer spray

  • INGREDIENTS AND APPEARANCE
    5ML HAND SANITIZER 
    5ml hand sanitizer spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75273-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75273-007-015 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - YIWU BAOLINA COSMETIC CO., LTD (528943389)
    Establishment
    NameAddressID/FEIBusiness Operations
    YIWU BAOLINA COSMETIC CO., LTD528943389manufacture(75273-007)