Label: JUVEHEAL HYDRO SYNERGY INTENSIVE SERUM- niacinamide, adenosine liquid
- NDC Code(s): 81689-060-01, 81689-060-02
- Packager: J MEDICAL Inter Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 16, 2022
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- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Sea Water, Water, Glycerin, Centella Asiatica Extract, 1,2-Hexanediol, Butylene Glycol, Xylitylglucoside, Sodium Hyaluronate, Hydroxypropyltrimonium Hyaluronate, Glutathione, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Hyaluronic Acid, Potassium Hyaluronate, Hydrolyzed Collagen, Elastin, Collagen Amino Acids, Palmitoyl Tripeptide-1, Palmitoyl Tripeptide-5, Acetyl Tetrapeptide-3, Acetyl Tetrapeptide-5, Tripeptide-1, Leucine, Phenylalanine, Arginine, Lysine HCl, Proline, Aspartic Acid, Valine, Isoleucine, Threonine, Histidine, Serine, Alanine, Anhydroxylitol, Xylitol, Glucose, Allantoin, Panthenol, Trehalose, Beta-Glucan, Aloe Barbadensis Leaf Extract, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Caprylic/Capric Triglyceride, Sorbitan Sesquioleate, Chlorphenesin, Xanthan Gum, Carbomer, Caprylyl Glycol, Ethylhexylglycerin
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other information
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JUVEHEAL HYDRO SYNERGY INTENSIVE SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81689-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2.0 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) 1,2-Hexanediol (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81689-060-02 1 in 1 CARTON 08/01/2022 1 NDC:81689-060-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2022 Labeler - J MEDICAL Inter Co., Ltd. (694065206) Registrant - J MEDICAL Inter Co., Ltd. (694065206) Establishment Name Address ID/FEI Business Operations J MEDICAL Inter Co., Ltd. 695439825 manufacture(81689-060)
