Label: N69 CUNT liquid

  • 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 October 8, 2020

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

  • Active Ingredient

    ETHYL ALCOHOL80%

  • Purpose

    Solven

  • Uses

    external usage products, spray on neck , wrist and other surfaces of skin .

  • Warnings

    1.Caution for those who are allergic to ethanol (alcohol).
    2.Should be stored in a cool and dry place, away from fire.
    3.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.
    In case of contact, rinse eyes thoroughly with water.

  • 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.(40℃)

  • Inactive ingredients

    AQUA, PARFUM

  • Package Label - Principal Display Panel

    74761-013-01 50ml

  • INGREDIENTS AND APPEARANCE
    N69 CUNT 
    n69 cunt liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74761-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DISPERSE RED 15 (UNII: 15FG1M8OP9)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74761-017-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product09/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/15/2020
    Labeler - Guangzhou Oumiao Cosmetics Co. Ltd.  (529806412)
    Registrant - Guangzhou Oumiao Cosmetics Co. Ltd.  (529806412)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Oumiao Cosmetics Co. Ltd.    529806412manufacture(74761-017)