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PUREFORET Brightening by ECOCATION Co., Ltd.

Dosage form: cream
Ingredients: GLYCERIN 1g in 100mL
Labeler: ECOCATION Co., Ltd.
NDC Code: 71600-008

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.

Active ingredient



Hibiscus flower extracts is rich in vitamin C, which helps skin fair and radiant. PUREFORET BRIGHTENING TONER is made with beeswax, shea butter, and vitamin E etc to nourish the skin and give a boost


Gently apply over the whole face

For external use only. Avoid contact with eyes

Discontinue use if signs of irritation and/or rash appear

Keep out of reach of children

Keep out of reach of children

Keep out of reach of children


For external use only


Hibiscus Rosa-Sinensis Flower Extract, Propanediol, Helianthus Annuus (Sunflower) Seed Oil, Sodium hyaluronate, Macadamia Ternifolia Seed Oil, Beeswax, Polysorbate 80, 1,2-Hexanediol, rh-Oligopeptide-1, Butyrospermum Parkii (Shea) Butter, Glyceryl Stearate, Opuntia Coccinellifera, Centella Asiatica Extract, Propolis Extract, Angelica gigas root extract, Aloe Barbadensis Leaf Extract, Caviar Extract, Rose Extract, Paeonia Albiflora Root Extract, Lilium Candidum Flower Extract, Rehmannia Chinensis Root Extract, Nelumbo Nucifera Seed Extract, Polygonatum Officinale Rhizome/Root Powder, Trehalose, Pinus Thunbergii Leaf Extract, Camellia sinensis leaf Extract, Ginkgo Biloba Leaf Extract, Houttuynia Cordata Extract, Laminaria Japonica Extract, Cucumis Sativus (Cucumber) Fruit Extract, Tocopheryl Acetate, Panthenol, Allantoin, Simmondsia Chinensis (Jojoba) Seed Oil, Lecithin, Sorbitan Sesquioleate, Sodium Polyacrylate, Hydrogenated Polydecene, Cetearyl Alcohol, Stearic Acid, Arginine, Carbomer, Ethylhexylglycerin, Lavandula Angustifolia (Lavender) Oil, Pelargonium Graveolens Flower Oil, Rose Flower Oil, Cymbopogon Martini Oil

glycerin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71600-008
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:71600-008-0150 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34708/01/2017
Labeler - ECOCATION Co., Ltd. (689845861)
Registrant - ECOCATION Co., Ltd. (689845861)
ECOCATION Co., Ltd.689845861label(71600-008), manufacture(71600-008)

Revised: 08/2017

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.