Label: HYALURONIC ACID MICRO- hyaluronate sodium patch

  • NDC Code(s): 70018-010-01
  • Packager: JUNMOK INTERNATIONAL,INC
  • 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 6, 2015

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

  • ACTIVE INGREDIENT

    Active Ingredient: Sodium hyaluronate 95.0%

    Close
  • INACTIVE INGREDIENT

    Inactive Ingredient: Lactose

    Close
  • PURPOSE

    Purpose: Skin Protectant

    Close
  • WARNINGS

    Warnings: 1. Do not use if irritation occurs. 2. Avoid using on sensitive skin. 3. Keep out of reach of children 4. For external use only. 5. Store in a cool place

    Close
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of babies and children

    Close
  • INDICATIONS & USAGE

    Indications & usage:1. Take a patch out of the pouch with dry hand after face washing. 2. Try not to touch the middle side (needle) and take off the protective film carefully. 3. Place and attach the middle side of the patch on a desired area vertically. 4. Press the middle part of the patch attached with fingers several times. 5. Go to bed with patch attached and take it off the next morning.

    Close
  • DOSAGE & ADMINISTRATION

    Dosage & Administration: 2-3 times a week.

    Close
  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
  • INGREDIENTS AND APPEARANCE
    HYALURONIC ACID MICRO 
    hyaluronate sodium patch
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:70018-010
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 1.14 g  in 4 
    Inactive Ingredients
    Ingredient Name Strength
    Lactose (UNII: J2B2A4N98G)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70018-010-01 4 in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 07/01/2015
    Labeler - JUNMOK INTERNATIONAL,INC (689045829)
    Registrant - JUNMOK INTERNATIONAL,INC (689045829)
    Establishment
    Name Address ID/FEI Business Operations
    JUNMOK INTERNATIONAL,INC 689045829 manufacture(70018-010)
    Close