Label: DR.NUELL PROPOLIS REAL 90 AMPOULE- glycerin 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 November 3, 2019

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

  • ACTIVE INGREDIENT

    glycerin

  • PURPOSE

    a multi ampoule for high-moisturizing & high-nourishing

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    Please refer to the instructions on the package.

  • WARNINGS

    1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
    2) Do not use for wounded areas
    3) Precautions for storage and handling
    keep out of reach of children, store away from direct sunlight
    4) avoid the eye area

  • INACTIVE INGREDIENT

    butylene glycol, sodium hyaluronate, arginine, etc

  • DOSAGE & ADMINISTRATION

    For external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DR.NUELL PROPOLIS REAL 90 AMPOULE 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73430-0004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73430-0004-1100 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34711/01/2019
    Labeler - Apharm Co., Ltd. (689054266)
    Registrant - Apharm Co., Ltd. (689054266)
    Establishment
    NameAddressID/FEIBusiness Operations
    APHARM Co., Ltd.689054266manufacture(73430-0004)