- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water, Butylene Glycol, Sodium Hyaluronate, Niacinamide, Silica, Polyglutamic acid, Methionine, Serine, Histidine, 1,2-Hexandiol, Hydroxyethylethylcelluose, Propylene Glycol, Camellia Sinensis Leaf Extract, Citrus Aurantium Bergamia (Bergamot) Leaf Extract, Lavendula Angustifolia (Lavender) Flower Extract, Rosa Centifolia Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Glycerin, Calcium Pantothenate, Sodium Ascorbyl Phosphate, Tocopheryl Acetate, Pyridoxine HCl, Maltodextrin/ Sodium Starch Octenylsuccinate, Sodium Hydroxide, Octanediol, Ethylhexylglycerin, Citrus grandis (grapefruit) seed extract, Artemisia princeps extract, Carbomer, Polysorbate 80, Dryopteris Filix-Mas Root Extract, Allantoin, Centella Asiatica Extract, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (matricaria) Flower Extract, Portulaca Oleracea Extract, Belamcanda Chinensis Root Extract, Dipotassium Glycyrrhizate, Xanthan Gum, Adenosine, Vanillyl butyl ether, Fragrance, Disodium EDTA
- PURPOSE
-
WARNINGS
For skin use only.
Do not use
on puncture wounds on animal bites on serious burns on area with scratches, eczema, or dermatitis
When using this product
avoid contact with eyes
Stop use and ask a doctor if
you have allergy or skin disease
rash or irritation develops and lasts
red spots, swelling, itching, irritation and other abnormalities develops - KEEP OUT OF REACH OF CHILDREN SECTION
- INDICATIONS & USAGE SECTION
- DOSAGE & ADMINISTRATION SECTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
T2 SERUM
allantoin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71327-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin 0.000003 g in 30 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Methionine (UNII: AE28F7PNPL) Serine (UNII: 452VLY9402) Histidine (UNII: 4QD397987E) Propylene Glycol (UNII: 6DC9Q167V3) Maltodextrin (UNII: 7CVR7L4A2D) Sodium Hydroxide (UNII: 55X04QC32I) Polysorbate 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71327-008-01 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/20/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/20/2017 Labeler - MICELL KOREA CO.,LTD (689851542) Registrant - MICELL KOREA CO.,LTD (689851542) Establishment Name Address ID/FEI Business Operations MICELL KOREA CO.,LTD 689851542 manufacture(71327-008)