Label: DAILYGARD HAND SANITIZER PE BOTTLE (SCREW CAP)- alcohol liquid

  • Contains inactivated NDC Code(s)
    NDC Code(s):     75749-014-01, 75749-014-02, 75749-014-03, 75749-014-04, view more
    75749-014-05, 75749-014-06, 75749-014-07, 75749-014-08, 75749-014-09, 75749-014-10, 75749-014-11, 75749-014-12
  • Packager: Ningbo Pretty Tourism Manufacturer Co. Ltd.
  • 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 May 11, 2020

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  • Active Ingredient(s)

    Ethyl Alcohol 70% Purpose: Antimicrobial

  • Purpose

    Antimicrobial

  • Uses

    Use(s)

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    Warnings

    For external use only. Flammable, Keep away from heat or flame

    Do not use

    • on infants
    • on open skin wounds

    When using this product

    • Keep out of eyes, ears, and mouth
    • In case of contact with eyes, rinse eyes thoroughly with water
  • STOP USE

    • Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious conditions.
  • 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

    • Apply as needed into palm of hand and thoroughly spread on both hands, rub unitl dry.
    • Supervise children under 6 years of age when using this product
  • Other information

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

    Deionized water, Triethanolamine, Carbomer, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

  • Package Label - Principal Display Panel

    100 ml

  • PRINCIPAL DISPLAY PANEL

    1000

  • PRINCIPAL DISPLAY PANEL

    500

  • PRINCIPAL DISPLAY PANEL

    5

  • PRINCIPAL DISPLAY PANEL

    250

  • PRINCIPAL DISPLAY PANEL

    237

  • PRINCIPAL DISPLAY PANEL

    2.5

  • PRINCIPAL DISPLAY PANEL

    60

  • PRINCIPAL DISPLAY PANEL

    1 gallon

  • PRINCIPAL DISPLAY PANEL

    label

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DAILYGARD HAND SANITIZER  PE BOTTLE (SCREW CAP)
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75749-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 L  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75749-014-011 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    2NDC:75749-014-022 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    3NDC:75749-014-032.5 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    4NDC:75749-014-045 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    5NDC:75749-014-056 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    6NDC:75749-014-0610 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    7NDC:75749-014-0712.5 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    8NDC:75749-014-0815 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    9NDC:75749-014-0920 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    10NDC:75749-014-1025 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    11NDC:75749-014-1128 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    12NDC:75749-014-1230 L in 1 BOTTLE; Type 0: Not a Combination Product04/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/23/2020
    Labeler - Ningbo Pretty Tourism Manufacturer Co. Ltd. (553193489)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Pretty Tourism Manufacturer Co. Ltd.553193489manufacture(75749-014)
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