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PUREFORET Skin balancing

Dosage form: lotion
Ingredients: GLYCERIN 4g in 100mL
Labeler: ECOCATION Co., Ltd.
NDC Code: 71600-001

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

glycerin

Purpose

refreshing skin refining pairing that sweeps away dulling surface impurities

Use

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

Directions

for external use only

INACTIVE INGREDIENT

Papaver Rhoeas Seed Extract, Propanediol, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Macadamia Ternifolia Seed Oil, 1,2-Hexanediol, rh-Oligopeptide-1, Sodium hyaluronate, Betaine, Isopropyl Myristate, Anthemis Nobilis Flower Extract, Portulaca Oleracea Extract, Centella Asiatica Extract, Polygonum Multiflorum Root Extract, Caviar Extract, Phellinus Linteus Extract, 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, Simmondsia Chinensis (Jojoba) Seed Oil, Allantoin, Polysorbate 80, Cetearyl Alcohol, Sorbitan Sesquioleate, Sodium Polyacrylate, Hydrogenated Polydecene, Lecithin, Carbomer, Arginine, Disodium EDTA, Ethylhexylglycerin, Citrus Nobilis (Mandarin Orange) Peel Oil, Pelargonium Graveolens Flower Oil, Citrus Aurantium Amara (Bitter Orange) Flower Oil

PUREFORET SKIN BALANCING 
glycerin lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71600-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:71600-001-01150 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)
Establishment
NameAddressID/FEIOperations
ECOCATION Co., Ltd.689845861manufacture(71600-001), label(71600-001)

Revised: 08/2017
 
ECOCATION Co., Ltd.

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.

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