Label: MEDI HYDRO DP TONER- glycerin liquid

  • 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 January 24, 2019

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  • INDICATIONS & USAGE

    Apply enough amount using cotton pad or hand and allow it to absorb, every day and night after face wash

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    for external use only

  • WARNINGS

    Discontinue use of the product if any of the following symptoms occurred. Consult a dermatologist if the symptoms got worse.
    a) If redness, Swelling, Itchiness, Irritation occurred during using.
    b) If the above symptoms started to occur when exposed to direct sunlight.
    Do not use on skins with wounds, eczema or dermatitis.

    Storage instructions
    a) Always close the lid after finish using.
    b) Store in a safe place away and out of reach of children.
    c) Store in a place with not too high or low temperature, keep awayfrom direct sunlight exposure.

  • PURPOSE

    Covers and protects sensitive skin with its fresh and moisturizing effects.

  • INACTIVE INGREDIENT

    water, butylene glycol, niacinamide, hyaluronic acid, etc.

  • ACTIVE INGREDIENT

    glycerin

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MEDI HYDRO DP TONER 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70694-0006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70694-0006-1130 mL in 1 BOTTLE; Type 0: Not a Combination Product01/24/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34701/24/2019
    Labeler - Inc MBG (688436167)
    Establishment
    NameAddressID/FEIBusiness Operations
    Inc MBG688436167manufacture(70694-0006)
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