- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Methylpropanediol, Butylene Glycol, Glycerin, Dipropylene Glycol, Chamomilla Recutita (Matricaria) Flower Extract, Acer saccharum (Sugar Maple) Extract, Portulaca Oleracea Extract, Betaine, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Ethylhexylglycerin, Xanthan Gum, Polysorbate 60, Sorbitan Isostearate, Ascorbyl Glucoside, Fragrance, Sodium Hyaluronate, Artemisia Capillaris Flower Extract, Ecklonia Cava Extract, Houttuynia Cordata Extract, Ledum Palustre Extract, Saururus Chinensis Extract, Tocopheryl Acetate, Triethanolamine, Achillea Millefolium Extract, Arnica Montana Flower Extract, Artemisia Absinthium Extract, Gentiana Lutea Root Extract, Palmitoyl Tripeptide-5.
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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Directions
Directions: 1) Clean and dry face. 2) Remove mask from package and gently unfold. 3) Place mask directly on skin, contouring it to fit the curves around the eyes, nose and mouth. 4) Leave on for 10-20 minutes. 5) Remove mask and gently pat the face with fingertips until the remaining serum is fully absorbed. *Suggested use is 2-3 times a week.
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Directions
Directions: 1) Clean and dry face. 2) Remove mask from package and gently unfold. 3) Place mask directly on skin, contouring it to fit the curves around the eyes, nose and mouth. 4) Leave on for 10-20 minutes. 5) Remove mask and gently pat the face with fingertips until the remaining serum is fully absorbed. *Suggested use is 2-3 times a week.
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VITA BRIGHTENING RENEWAL MASK
witch hazel patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69424-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Witch Hazel (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) Witch Hazel 0.025 mg in 25 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69424-030-01 25 mL in 1 CELLO PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/02/2015 Labeler - SANSUNG LIFE & SCIENCE CO., LTD. (689524929) Registrant - SANSUNG LIFE & SCIENCE CO., LTD. (689524929) Establishment Name Address ID/FEI Business Operations SANSUNG LIFE & SCIENCE CO., LTD. 689524929 manufacture(69424-030)