Label: GEM BEAUTY AMETHYST INTENSIVE FIRMING EYE CREAM- aloe vera flower cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 9, 2009

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

View All Sections
  • ACTIVE INGREDIENT

    INGREDIENTS:

    Aloe Ferox Leaf Extract, Rosa Hybrid Flower Extract, Chamomilla Recutitia [Matricaria] Flower Extract, Geranium Maculatum Extract, Rosa Canina Fruit Oil, Shea Butter, Collagen, Honey, Silk Amino Acids, Cotton Seed Oil, Carmellia Sinensis Seed Oil, Ceramide, Arbutin, Amethyst Powder, Grapefruit Fruit Extract, Cellulose Gum, Tocopherol, Adenosine, Fragrance

  • WARNINGS

    WARNINGS:

    If any adverse reactions occur such as swelling, itching or skin irritation, stop using and consult a doctor immediately.  Avoid use in wounds or around eyes.  For external use only.  Please try not to get this cream into your eyes.

  • WHEN USING

    DIRECTIONS:

    Gently part a small amount around your eye area after cleansing and moisturizing.

  • STORAGE AND HANDLING

    STORAGE:

    Keep out of reach of children.  Store in a cool place and avoid excessive heat.  Seal tightly for further use.  Do not use if seal under cap is broken or missing.

  • PRINCIPAL DISPLAY PANEL

    LABEL
  • INGREDIENTS AND APPEARANCE
    GEM BEAUTY AMETHYST INTENSIVE FIRMING EYE CREAM 
    aloe vera flower cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50030-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALOE VERA FLOWER (UNII: 575DY8C1ER) (ALOE VERA FLOWER - UNII:575DY8C1ER) ALOE VERA FLOWER5.4 mL  in 30 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50030-001-0130 mL in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart310.54512/01/2009
    Labeler - GEMPARK CO LTD (690232116)
    Registrant - GEMPARK CO LTD (690232116)
    Establishment
    NameAddressID/FEIBusiness Operations
    GEMPARK CO LTD690232116manufacture
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, PubMed, Biochemical Data Summary

More Info on this Drug

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