Label: LA FACE ALL IN ONE- 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 June 21, 2018

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Glycerin, Niacinamide, Adenosine

  • INACTIVE INGREDIENT

    Water, Butylene Glycol, etc.

  • PURPOSE

    Skin Protectant - Elasticity, Skin Whitening & Wrinkle Improvement

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Spray La face All in One evenly on entire face after cleansing. Spread gently with your fingers until it is fully absorbed. You can repeat this process as needed.

  • WARNINGS

    1. Discontinue use and ask a doctor if any adverse reactions occur such as rash, swelling or irritation after use or due to direct sunlight.
    2. Do not use on damaged or broken skin.
    3. Storage and Handling Precautions

    (A)Keep out of reach of children.

    (B)Keep out of direct sunlight.

    4. Avoid contact with eyes.

    If there is any problem with this product, compensation is offered by based on ‘Consumer Dispute Resolution Criteria’, notice by The Fair Trade Commission.

    Customer Support Center +82-2-512-0478

  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    LA FACE ALL IN ONE 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72312-0011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72312-0011-250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34706/01/2018
    Labeler - CELLALAB (690452262)
    Registrant - CELLALAB (690452262)
    Establishment
    NameAddressID/FEIBusiness Operations
    SAMSUNG MEDICOS. CO., LTD. Hyangnam Factory689851701manufacture(72312-0011)
    Establishment
    NameAddressID/FEIBusiness Operations
    CELLALAB690452262relabel(72312-0011)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!