Label: WEDOL WATER-BASED PERSONAL LUBRICANT- water-based personal lubricant oil

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated August 16, 2019

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  • active ingredient

    active ingredient

  • indication usage

    instruction

  • instructions for use

    instruction for use

  • inactive

    inactive

  • ask a doctor

    ask a doctor

  • warnings

    warning

  • stop using

    stop use

  • when using

    when using

  • keep out of

    keep out of children

  • dosage

    dosage

  • purpose

    purpose

  • package

    package

  • INGREDIENTS AND APPEARANCE
    WEDOL WATER-BASED PERSONAL LUBRICANT 
    water-based personal lubricant oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73298-190
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5) (HYDROXYETHYL CELLULOSE (140 CPS AT 5%) - UNII:8136Y38GY5) HYDROXYETHYL CELLULOSE (140 CPS AT 5%)3.84 g  in 240 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEG-7 DISTEARATE (UNII: VU1ZWG290C) 1.2 mL  in 240 mL
    WATER (UNII: 059QF0KO0R) 186 mL  in 240 mL
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 0.72 mL  in 240 mL
    CHLORPHENESIN (UNII: I670DAL4SZ) 0.192 mL  in 240 mL
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 48 mL  in 240 mL
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73298-190-341 in 1 BOX09/15/2019
    1NDC:73298-190-33240 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/15/2019
    Labeler - Shenzhenshi Huaxiang Technology Co.,Ltd. (554499381)
    Registrant - Shenzhenshi Huaxiang Technology Co.,Ltd. (554499381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhenshi Huaxiang Technology Co.,Ltd.554499381label(73298-190) , manufacture(73298-190)