Label: ASLDAN HAND DISINFECTION 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 July 27, 2020

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  • Active Ingredient(s)

    Ethyl Alcohol 75% v/v

  • Purpose

    Antimicrobia

  • Use

    For hand washing to decrease bacteria on the skin· Recommended for repeated use.

  • Warnings

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

  • Do not use

    Do not use in the eyes. In case of contact,rinse eyes thoroughly with water.

  • WHEN USING

    /

  • STOP USE

    Stop use and ask a doctor if irritation and redness develops and 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 briskly and rub hands together until dry
    Supervise children under 6 years in the use of this product

  • Other information

  • Inactive ingredients

    Water

  • Package Label - Principal Display Panel

    500805000120501502001000300100

  • INGREDIENTS AND APPEARANCE
    ASLDAN HAND DISINFECTION 
    asldan hand disinfection spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79865-002
    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
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79865-002-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    2NDC:79865-002-0280 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    3NDC:79865-002-03100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    4NDC:79865-002-04120 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    5NDC:79865-002-05150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    6NDC:79865-002-06200 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    7NDC:79865-002-07300 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    8NDC:79865-002-08500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    9NDC:79865-002-091000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
    10NDC:79865-002-105000 mL in 1 BOTTLE; 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 - Guangdong Keying Technology Co., Ltd (553032880)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Keying Technology Co., Ltd553032880manufacture(79865-002)