Label: HAND SANITIZER- ethyl alcohol gel

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    73357-627-00, 73357-627-01, 73357-627-02, 73357-627-03, view more
    73357-627-05, 73357-627-08, 73357-627-09, 73357-627-10, 73357-627-15, 73357-627-20, 73357-627-24, 73357-627-25, 73357-627-29, 73357-627-30, 73357-627-35, 73357-627-50, 73357-627-51, 73357-627-55, 73357-627-60, 73357-627-80
  • Packager: Hangzhou Lanqueen Cosmetics 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 April 10, 2020

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

  • Drug Facts

  • Active Ingredients:

    Ethyl alcohol 62%

  • PURPOSE

    Antiseptic

  • Uses:

    Hand sanitizer

  • Warning:

    For external use only.

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

    Discontinue if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

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

  • Directions:

    Place enough product in palm to cover hands and rub hands together briskly until dry.

  • Inactive Ingredients:

    Purified Water, Glycerin, Triethanolamine, Carbomer fragrance, Vitamin E, Aloe Vera.

  • SPL UNCLASSIFIED SECTION

    Made in China

  • Packaging

    sanitizer1

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73357-627
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73357-627-1010 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    2NDC:73357-627-1515 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    3NDC:73357-627-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    4NDC:73357-627-6060 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    5NDC:73357-627-8080 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    6NDC:73357-627-00100 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    7NDC:73357-627-088 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    8NDC:73357-627-2929 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    9NDC:73357-627-20120 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    10NDC:73357-627-50150 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2019
    11NDC:73357-627-0550 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    12NDC:73357-627-02200 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    13NDC:73357-627-24240 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    14NDC:73357-627-25250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    15NDC:73357-627-03300 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    16NDC:73357-627-35350 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    17NDC:73357-627-51500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    18NDC:73357-627-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    19NDC:73357-627-555 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    20NDC:73357-627-0990 mL in 1 BOTTLE; Type 0: Not a Combination Product03/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/15/2019
    Labeler - Hangzhou Lanqueen Cosmetics Co., Ltd. (542984409)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hangzhou Lanqueen Cosmetics Co., Ltd.542984409manufacture(73357-627)