Label: HYDRATING MOISTURE DAY AND NIGHTCREAM- citronellol, geraniol cream

  • NDC Code(s): 71217-0071-1, 71217-0071-2, 71217-0071-3
  • Packager: inthismorning co ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 13, 2023

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  • ACTIVE INGREDIENT

    citronellol, geraniol

  • INACTIVE INGREDIENT

    water, glycerin, etc

  • PURPOSE

    moisturizing, whitening, wrinkle care

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    apply proper amount to the skin

  • WARNINGS

    This product is for exeternal use only. Do not use for internal use
    Storage and handling precautions
    If possible, avoid direct sunlight and store in cool and area of low humidity in order to maintain the quality of the product and avoid misuse
    Avoid placing the product near fire and store out in reach of children

    - consult a physician in case of abnormal symptoms, such as red spots, swelling or itching, or side effects in the areas of application due to direct light during or after using the product

    - do not use on wounded area

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    HYDRATING MOISTURE DAY AND NIGHTCREAM 
    citronellol, geraniol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71217-0071
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) (.BETA.-CITRONELLOL, (R)- - UNII:P01OUT964K) .BETA.-CITRONELLOL, (R)-0.0090402 g  in 100 mL
    GERANIOL (UNII: L837108USY) (GERANIOL - UNII:L837108USY) GERANIOL0.003019275 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71217-0071-115 mL in 1 TUBE; Type 0: Not a Combination Product01/15/2023
    2NDC:71217-0071-250 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2023
    3NDC:71217-0071-3120 mL in 1 TUBE; Type 0: Not a Combination Product01/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/15/2023
    Labeler - inthismorning co ltd (695126076)
    Registrant - inthismorning co ltd (695126076)
    Establishment
    NameAddressID/FEIBusiness Operations
    cosmax inc689049693manufacture(71217-0071)
    Establishment
    NameAddressID/FEIBusiness Operations
    inthismorning co ltd695126076label(71217-0071)
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