Label: HAND SANITIZER liquid

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    75701-007-01, 75701-007-02, 75701-007-03, 75701-007-04, view more
    75701-007-05, 75701-007-06, 75701-007-07, 75701-007-08, 75701-007-09, 75701-007-10
  • Packager: Ningbo dingchi Intelligent Manufacturing Technology 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 March 10, 2021

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

  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

    Hand Sanitizer to help reduce bacteria on skin.

  • 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 doctor if irritation or rash appears and lasts.
    Keep out of reach for children. If swallowed, get medical help or contact a

    Poison Control Center right away.

  • Do not use

    do not use in or near the eyes.

  • When using this product

    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 doctor if irritation or rash appears and lasts.

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

  • STOP USE

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

  • Keep out of reach of children.

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

  • Directions

    Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
    Children under 6 years of age should be supervised when using this product.

  • Other information

    Store below 106°F. (41°C)
    May discolor certain fabrics or surfaces

  • Inactive ingredients

    Water(Aqua),Aloe Barbadensis Leaf Juice,Carbomer,Fragrance, Glycerin,Propylene Glycol,Tocopheryl Acetate,Triethanolamine, 2-(Dimethylamino) Ethanol.

  • Package Label - Principal Display Panel

    75701-007-04 80ml75701-007-08 1000ML75701-007-05 100ml75701-007-02 54ml75701-007-03 60ml75701-007-10 3780ML75701-007-01 30ml75701-007-06 237ml75701-007-07 500ML75701-007-09 1800ML

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75701-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    DEANOL (UNII: 2N6K9DRA24)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75701-007-05100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    2NDC:75701-007-103780 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    3NDC:75701-007-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    4NDC:75701-007-07500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    5NDC:75701-007-06237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    6NDC:75701-007-081000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    7NDC:75701-007-091800 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    8NDC:75701-007-0254 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    9NDC:75701-007-0360 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    10NDC:75701-007-0480 mL in 1 BOTTLE; Type 0: Not a Combination Product04/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/24/2020
    Labeler - Ningbo dingchi Intelligent Manufacturing Technology Co., Ltd. (554530925)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo dingchi Intelligent Manufacturing Technology Co., Ltd.554530925manufacture(75701-007)