Label: DIVILOO 75 PERCENT ALCOHOL DISINFECTANT- alcohol spray

  • Category: HUMAN OTC DRUG LABEL

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 16, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • SPL UNCLASSIFIED SECTION

    NA

  • Active Ingredient(s)

    Ethyl Alcohol 75% v/v

  • Purpose

    Antimicrobial

  • Use

    Hand Sanitizer to decrease bacteria on the skin that could cause disease

  • Warnings

    For external use only. Hands

    Flammable. Keep away from heat and flame

  • WHEN USING

    When using this product, avoid contacting with face, eyes, and broken skin. In case of eye contacting, flush with plenty of water and seek medical advice.

  • STOP USE

    Stop use and consult a doctor if irritation or redness occurs.

  • 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

    Rub hands thoroughly with this product until dry

    Children younger than 6 should be supervised by an adult when using

  • Other information

    Do not store above 105F

    May discolor some fabrics

    Harmful to wood finishes and plastics

    This product was not tested on animals

  • Inactive ingredients

    Water

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    DIVILOO 75 PERCENT ALCOHOL DISINFECTANT 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77937-002
    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:77937-002-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    2NDC:77937-002-0250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    3NDC:77937-002-0360 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    4NDC:77937-002-04100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    5NDC:77937-002-05236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    6NDC:77937-002-06300 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    7NDC:77937-002-07500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    8NDC:77937-002-08887 mL in 1 BOTTLE; Type 0: Not a Combination Product05/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/16/2020
    Labeler - Yiwu Weinimei (For Your Beauty) Cosmetics Co.,Ltd. (530881726)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yiwu Weinimei (For Your Beauty) Cosmetics Co.,Ltd.530881726manufacture(77937-002)