Label: RECOVERY BALM- arbutin, adenosine liquid

  • 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 January 3, 2020

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

  • ACTIVE INGREDIENT

    Arbutin, Adenosine

  • INACTIVE INGREDIENT

    Water, Butylene Glycol, etc.

  • PURPOSE

    Skin Protectant

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    How To Use: Take moderate amount and spread it over desired area for natural skin tone evenly.

    It can be used as regenerative cream for irritated skin or after peeling. You can apply it before sleeping due to excellent regenerative effect.

  • WARNINGS

    Precautions

    1. If the cosmetic causes red rash, swollenness or itching by exposure to sunlight during the use, you are advised to stop using it immediately and you may consult a pharmacist or a doctor

    2. It is not advised to use the cosmetic on the skin where you have scars

    3. Precautions for storage

    ⓐ Keep it out of infants or children’s reach

    ⓑ Keep it out of the place where exposure to direct sunlight exists

  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    RECOVERY BALM 
    arbutin, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72368-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN2 g  in 100 mL
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72368-0003-150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2018
    Labeler - Threedayslove Co., Ltd. (693724138)
    Registrant - Threedayslove Co., Ltd. (693724138)
    Establishment
    NameAddressID/FEIBusiness Operations
    Threedayslove Co., Ltd.693724138manufacture(72368-0003) , pack(72368-0003) , label(72368-0003)