NDC | 71727-104-01, 71727-104-02 |
Set ID | 8169d809-47a5-3f1e-e053-2991aa0a955c |
Category | HUMAN OTC DRUG LABEL |
Packager | iMode Korea, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use when skin is red, inflamed, irritated, or painful
When using this product
- do not apply on other parts of the body avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
- do not apply directly to wound or open cut
Stop use and ask a doctor if
- Rash or irritation on skin develops and lasts
- Keep out of reach of children
- Directions
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Inactive ingredients
Water, Glycerin, Butylene Glycol, Ceratonia Siliqua (Carob) Gum, Sucrose, Sodium Hyaluronate, Ethylhexylglycerin, Hydrolyzed Collagen, Simmondsia Chinensis (Jojoba) Seed Oil, Euterpe Oleracea Fruit Oil, Helianthus Annuus (Sunflower) Seed Oil, Tocopherol, Vitis Vinifera (Grape) Vine Extract, Carrageenan, Potassium Chloride, Xanthan Gum, Cellulose Gum, Sodium Polyacrylate, Dipotassium Glycyrrhizate, Gellan Gum, Calcium Lactate, PEG-60 Hydrogenated Castor Oil, Disodium EDTA, Chlorphenesin, Propanediol, Pentylene Glycol, Cocos Nucifera (Coconut) Fruit Extract, Pinus Sylvestris Leaf Extract, Ethyl Hexanediol, 1,2-Hexanediol
- Puriface Spirulina Eye Gel Masks
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INGREDIENTS AND APPEARANCE
PURIFACE SPIRULINA EYE GEL MASKS
spirulina platensis extract, allantoin patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71727-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.0864 g in 27 mL SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE) (SPIRULINA PLATENSIS - UNII:9L3TIH1UUE) SPIRULINA PLATENSIS 0.0675 g in 27 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71727-104-02 1 in 1 BOX 02/08/2019 1 NDC:71727-104-01 27 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/08/2019 Labeler - iMode Korea, Inc. (694627846) Registrant - iMode Korea, Inc. (694627846) Establishment Name Address ID/FEI Business Operations JINCOSTECH Co., Ltd. 688484870 manufacture(71727-104) Establishment Name Address ID/FEI Business Operations iMode Korea, Inc. 694627846 relabel(71727-104)